G. Attardi and G. Schatz, Biogenesis of Mitochondria, Annual Review of Cell Biology, vol.4, issue.1, pp.289-333, 1988.
DOI : 10.1146/annurev.cb.04.110188.001445

S. Ballinger, J. Shoffner, E. Hedaya, I. Trounce, M. Polak et al., Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion, Nature Genetics, vol.38, issue.1, pp.11-16, 1992.
DOI : 10.1016/0005-2728(90)90118-N

S. Bannwarth, M. Abbassi, R. Valéro, K. Fragaki, N. Dubois et al., A Novel Unstable Mutation in Mitochondrial DNA Responsible for Maternally Inherited Diabetes and Deafness, Diabetes Care, vol.34, issue.12, pp.2591-2594, 2011.
DOI : 10.2337/dc11-1012

S. Bannwarth, V. Procaccio, A. Lebre, C. Jardel, A. Chaussenot et al., Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders, Journal of Medical Genetics, vol.20, issue.10, pp.704-718, 2013.
DOI : 10.1136/jmedgenet-2013-101604

S. Bannwarth, V. Procaccio, and V. Paquis-flucklinger, Surveyor??? Nuclease: A new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defects, Human Mutation, vol.127, issue.6, pp.575-82, 2005.
DOI : 10.1002/humu.20177

C. Bayreuther, S. Hieronimus, P. Ferrari, P. Thomas, and C. Lebrun, Auto-immune cerebellar ataxia with anti-GAD antibodies accompanied by de novo late-onset type 1 diabetes mellitus, Diabetes & Metabolism, vol.34, issue.4, pp.386-394, 2008.
DOI : 10.1016/j.diabet.2008.02.002

E. Blakely, J. Yarham, C. Alston, K. Craig, J. Poulton et al., Pathogenic Mitochondrial tRNA Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease, Human Mutation, vol.85, issue.3, pp.1260-1268, 2013.
DOI : 10.1002/humu.22358

E. Cardaioli, D. Pozzo, P. Cerase, A. Sicurelli, F. Malandrini et al., Rapidly progressive neurodegeneration in a case with the 7472insC mutation and the A7472C polymorphism in the mtDNA tRNAser(UCN) gene, Neuromuscular Disorders, vol.16, issue.1, pp.26-31, 2006.
DOI : 10.1016/j.nmd.2005.11.001

I. Chamkha, E. Mkaouar-rebai, H. Aloulou, I. Chabchoub, C. Kifagi et al., A novel m.3395A>G missense mutation in the mitochondrial ND1 gene associated with the new tRNAIle m.4316A>G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss, Biochemical and Biophysical Research Communications, vol.404, issue.1, pp.504-514, 2011.
DOI : 10.1016/j.bbrc.2010.12.012

F. Chen, Y. Liu, X. Song, H. Hu, H. Xu et al., A novel mitochondrial DNA missense mutation at G3421A in a family with maternally inherited diabetes and deafness, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, vol.602, issue.1-2, pp.26-33, 2006.
DOI : 10.1016/j.mrfmmm.2006.07.006

J. Chen, Y. Hattori, K. Nakajima, T. Eizawa, T. Ehara et al., Mitochondrial complex I activity is significantly decreased in a patient with maternally inherited type 2 diabetes mellitus and hypertrophic cardiomyopathy associated with mitochondrial DNA C3310T mutation: A cybrid study, Diabetes Research and Clinical Practice, vol.74, issue.2, pp.148-53, 2006.
DOI : 10.1016/j.diabres.2006.03.024

A. Choo-kang, S. Lynn, G. Taylor, M. Daly, S. Sihota et al., Defining the Importance of Mitochondrial Gene Defects in Maternally Inherited Diabetes by Sequencing the Entire Mitochondrial Genome, Diabetes, vol.51, issue.7, pp.2317-2337, 2002.
DOI : 10.2337/diabetes.51.7.2317

M. Damore, P. Speiser, A. Slonim, M. New, S. Shanske et al., Early Onset of Diabetes Mellitus Associated with the Mitochondrial DNA T14709C Point Mutation: Patient Report and Literature Review, Journal of Pediatric Endocrinology and Metabolism, vol.12, issue.2, pp.207-220, 1999.
DOI : 10.1515/JPEM.1999.12.2.207

D. Block, C. , D. Leeuw, I. Maassen, J. Ballaux et al., A novel 7301-bp deletion in mitochondrial DNA in a patient with Kearns-Sayre syndrome, diabetes mellitus, and primary amenorrhoea, Exp Clin Endocrinol Diabetes. févr, vol.112, issue.2, pp.80-83, 2004.

L. Doleris, G. Hill, P. Chedin, D. Nochy, C. Bellanne-chantelot et al., Focal segmental glomerulosclerosis associated with mitochondrial cytopathy, Kidney International, vol.58, issue.5, pp.1851-1859, 2000.
DOI : 10.1111/j.1523-1755.2000.00356.x

X. Estivill, N. Govea, E. Barceló, C. Badenas, E. Romero et al., Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides, The American Journal of Human Genetics, vol.62, issue.1, pp.27-35, 1998.
DOI : 10.1086/301676

K. Gerbitz, K. Gempel, and D. Brdiczka, Mitochondria and Diabetes: Genetic, Biochemical, and Clinical Implications of the Cellular Energy Circuit, Diabetes, vol.45, issue.2, pp.113-139, 1996.
DOI : 10.2337/diab.45.2.113

K. Gerbitz, J. Van-den-ouweland, J. Maassen, and M. Jaksch, Mitochondrial diabetes mellitus: a review, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, vol.1271, issue.1, pp.253-60, 1995.
DOI : 10.1016/0925-4439(95)00036-4

B. Guéry, G. Choukroun, L. Noël, P. Clavel, A. Rötig et al., The Spectrum of Systemic Involvement in Adults Presenting with Renal Lesion and Mitochondrial tRNA(Leu) Gene Mutation, Journal of the American Society of Nephrology, vol.14, issue.8, pp.2099-108, 2003.
DOI : 10.1097/01.ASN.0000080180.51098.02

P. Guillausseau, D. Dubois-laforgue, P. Massin, M. Laloi-michelin, C. Bellanné-chantelot et al., Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD), Diabetes & Metabolism, vol.30, issue.2, pp.181-187, 2004.
DOI : 10.1016/S1262-3636(07)70105-2

P. Guillausseau, P. Massin, D. Dubois-laforgue, J. Timsit, M. Virally et al., Maternally Inherited Diabetes and Deafness: A Multicenter Study, Annals of Internal Medicine, vol.134, issue.9_Part_1, pp.721-729, 2001.
DOI : 10.7326/0003-4819-134-9_Part_1-200105010-00008

M. Hanna, I. Nelson, M. Sweeney, J. Cooper, P. Watkins et al., Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation, Am J Hum Genet. mai, vol.56, issue.5, pp.1026-1059, 1995.

H. Hao, E. Bonilla, G. Manfredi, S. Dimauro, and C. Moraes, Segregation patterns of a novel mutation in the mitochondrial tRNA glutamic acid gene associated with myopathy and diabetes mellitus, Am J Hum Genet. mai, vol.56, issue.5, pp.1017-1042, 1995.

Y. Hattori, M. Takeoka, K. Nakajima, T. Ehara, and M. Koyama, A Heteroplasmic Mitochondrial DNA 3310 Mutation in the ND1 Gene in a Patient with Type 2 Diabetes, Hypertrophic Cardiomyopathy, and Mental Retardation, Experimental and Clinical Endocrinology & Diabetes, vol.113, issue.6, pp.318-341, 2005.
DOI : 10.1055/s-2005-865646

Y. Hattori, K. Nakajima, T. Eizawa, T. Ehara, M. Koyama et al., Heteroplasmic Mitochondrial DNA 3310 Mutation in NADH Dehydrogenase Subunit 1 Associated With Type 2 Diabetes, Hypertrophic Cardiomyopathy, and Mental Retardation in a Single Patient, Diabetes Care, vol.26, issue.3, pp.952-955, 2003.
DOI : 10.2337/diacare.26.3.952

M. Hirai, S. Suzuki, M. Onoda, Y. Hinokio, A. Hirai et al., Mitochondrial deoxyribonucleic acid 3256C-T mutation in a Japanese family with noninsulindependent diabetes mellitus, J Clin Endocrinol Metab. mars, vol.83, issue.3, pp.992-996, 1998.

N. Hosszúfalusi, V. Karcagi, R. Horváth, E. Palik, J. Várkonyi et al., A detailed investigation of maternally inherited diabetes and deafness (MIDD) including clinical characteristics, C-peptide secretion, HLA-DR and -DQ status and autoantibody pattern, Diabetes/Metabolism Research and Reviews, vol.29, issue.2, pp.127-162, 2009.
DOI : 10.1002/dmrr.841

G. Hyde and E. Rubel, Mitochondrial role in hair cell survival after injury, Otolaryngology - Head and Neck Surgery, vol.113, issue.5, pp.530-570, 1995.
DOI : 10.1016/S0194-5998(95)70043-9

M. Jaksch, S. Hofmann, S. Kleinle, S. Liechti-gallati, D. Pongratz et al., A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy., Journal of Medical Genetics, vol.35, issue.11, pp.895-900, 1998.
DOI : 10.1136/jmg.35.11.895

K. Kameoka, H. Isotani, K. Tanaka, H. Kitaoka, and N. Ohsawa, Impaired insulin secretion in Japanese diabetic subjects with an A-to-G mutation at nucleotide 8296 of the mitochondrial DNA in tRNA(Lys) Diabetes Care, nov, vol.21, issue.11, pp.2034-2039, 1998.

A. Karaa and A. Goldstein, The spectrum of clinical presentation, diagnosis, and management of mitochondrial forms of diabetes, Pediatric Diabetes, vol.80, issue.Suppl 1, pp.1-9, 2015.
DOI : 10.1111/pedi.12223

H. Katagiri, T. Asano, H. Ishihara, K. Inukai, M. Anai et al., Mitochondrial diabetes mellitus: Prevalence and clinical characterization of diabetes due to mitochondrial tRNALeU(UUR) gene mutation in Japanese patients, Diabetologia, vol.17, issue.5, pp.504-514, 1994.
DOI : 10.1007/s001250050139

H. Liu, R. Li, W. Li, M. Wang, J. J. Zheng et al., Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNAGly gene, Mitochondrion, vol.21, pp.49-57, 2015.
DOI : 10.1016/j.mito.2015.01.004

S. Lynn, T. Wardell, M. Johnson, P. Chinnery, M. Daly et al., Mitochondrial diabetes: investigation and identification of a novel mutation, Diabetes, vol.47, issue.11, pp.1800-1802, 1998.
DOI : 10.2337/diabetes.47.11.1800

J. Maassen and T. Kadowaki, Maternally inherited diabetes and deafness: a new diabetes subtype, Diabetologia, vol.35, issue.4, pp.375-82, 1996.
DOI : 10.1007/BF00400668

J. Maassen, L. Hart, E. Van-essen, R. Heine, G. Nijpels et al., Mitochondrial Diabetes: Molecular Mechanisms and Clinical Presentation, Diabetes, vol.53, issue.Supplement 1, pp.103-112, 2004.
DOI : 10.2337/diabetes.53.2007.S103

J. Maassen, G. Janssen, and L. Hart, Molecular mechanisms of mitochondrial diabetes (MIDD), Annals of Medicine, vol.12, issue.1, pp.213-234, 2005.
DOI : 10.1038/ng0892-368

A. Maitra, Y. Cohen, S. Gillespie, E. Mambo, N. Fukushima et al., The Human MitoChip: A High-Throughput Sequencing Microarray for Mitochondrial Mutation Detection, Genome Research, vol.14, issue.5, pp.812-821, 2004.
DOI : 10.1101/gr.2228504

P. Massin, D. Dubois-laforgue, T. Meas, M. Laloi-michelin, H. Gin et al., Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case???control study, Diabetologia, vol.46, issue.9, pp.1664-70, 2008.
DOI : 10.1007/s00125-008-1073-1

P. Massin, P. Guillausseau, B. Vialettes, V. Paquis, F. Orsini et al., Macular Pattern Dystrophy Associated With a Mutation of Mitochondrial DNA, American Journal of Ophthalmology, vol.120, issue.2, pp.247-255, 1995.
DOI : 10.1016/S0002-9394(14)72615-7

P. Massin, M. Virally-monod, B. Vialettes, M. Paques, H. Gin et al., Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness, Ophthalmology, vol.106, issue.9, pp.1821-1828, 1999.
DOI : 10.1016/S0161-6420(99)90356-1

T. Meas, M. Laloi-michelin, M. Virally, C. Ambonville, J. Kevorkian et al., Diagnostic clinique et biologique du diab??te mitochondrial et particularit??s de sa prise en charge, La Revue de M??decine Interne, vol.31, issue.3, pp.216-237, 2010.
DOI : 10.1016/j.revmed.2008.11.017

N. Mezghani, E. Mkaouar-rebai, M. Mnif, N. Charfi, N. Rekik et al., The heteroplasmic m.14709T>C mutation in the tRNAGlu gene in two Tunisian families with mitochondrial diabetes, Journal of Diabetes and its Complications, vol.24, issue.4, pp.270-277, 2010.
DOI : 10.1016/j.jdiacomp.2009.11.002

K. Morten, J. Cooper, G. Brown, B. Lake, D. Pike et al., A new point mutation associated with mitochondrial encephalomyopathy, Human Molecular Genetics, vol.2, issue.12, pp.2081-2088, 1993.
DOI : 10.1093/hmg/2.12.2081

R. Murphy, D. Turnbull, M. Walker, and A. Hattersley, Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation, Diabetic Medicine, vol.17, issue.2, pp.383-99, 2008.
DOI : 10.1046/j.1526-4610.2000.00088.x

S. Nakano, M. Fukuda, F. Hotta, T. Ito, T. Ishii et al., Mitochondrial DNA Point Mutation at Nucleotide Pair 3316 in a Japanese Family with Heterogeneous Phenotypes of Diabetes., Endocrine Journal, vol.45, issue.5, pp.625-655, 1998.
DOI : 10.1507/endocrj.45.625

H. Narbonne and B. Vialettes, Les diabètes par cytopathie mitochondriale, Médecine thérapeutique / Endocrinologie. 29 juin, vol.2, issue.3, pp.217-245, 2000.

V. Nesbitt, R. Pitceathly, D. Turnbull, R. Taylor, M. Sweeney et al., The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management, Journal of Neurology, Neurosurgery & Psychiatry, vol.3, issue.8, pp.936-944, 2013.
DOI : 10.1136/jnnp-2012-303528

M. Odawara, K. Sasaki, and K. Yamashita, A G-to-A Substitution at Nucleotide Position 3316 in Mitochondrial DNA Is Associated with Japanese Non-Insulin-Dependent Diabetes Mellitus, Biochemical and Biophysical Research Communications, vol.227, issue.1, pp.147-51, 1996.
DOI : 10.1006/bbrc.1996.1481

K. Ohkubo, A. Yamano, M. Nagashima, Y. Mori, K. Anzai et al., Mitochondrial gene mutations in the tRNA(Leu(UUR)) region and diabetes: prevalence and clinical phenotypes in Japan, Clin Chem. sept, vol.47, issue.9, pp.1641-1649, 2001.

S. Otabe, K. Yasuda, Y. Mori, K. Shimokawa, H. Kadowaki et al., Molecular and Histological Evaluation of Pancreata from Patients with a Mitochondrial Gene Mutation Associated with Impaired Insulin Secretion, Biochemical and Biophysical Research Communications, vol.259, issue.1, pp.149-56, 1999.
DOI : 10.1006/bbrc.1999.0650

V. Paquis-flucklinger, B. Vialettes, P. Vague, B. Canivet, S. Hieronimus et al., Importance of searching for mtDNA defects in patients with diabetes and hearing deficit, Diabetologia, vol.41, issue.6, pp.740-741, 1998.
DOI : 10.1007/s001250050978

C. Pereira, C. Nogueira, C. Barbot, T. A. Soares, C. Fattori et al., Identification of a new mtDNA mutation (14724G>A) associated with mitochondrial leukoencephalopathy, Biochemical and Biophysical Research Communications, vol.354, issue.4, pp.937-978, 2007.
DOI : 10.1016/j.bbrc.2007.01.068

D. Perucca-lostanlen, H. Narbonne, J. Hernandez, P. Staccini, A. Saunieres et al., Mitochondrial DNA Variations in Patients with Maternally Inherited Diabetes and Deafness Syndrome, Biochemical and Biophysical Research Communications, vol.277, issue.3, pp.771-776, 2000.
DOI : 10.1006/bbrc.2000.3751

W. Reardon, R. Ross, M. Sweeney, L. Luxon, M. Pembrey et al., Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA, The Lancet, vol.340, issue.8832, pp.1376-1385, 1992.
DOI : 10.1016/0140-6736(92)92560-3

C. Richter, J. Park, and B. Ames, Normal oxidative damage to mitochondrial and nuclear DNA is extensive., Proceedings of the National Academy of Sciences, vol.85, issue.17, pp.6465-6472, 1988.
DOI : 10.1073/pnas.85.17.6465

L. Rigoli, F. Prisco, R. Caruso, D. Iafusco, G. Ursomanno et al., Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and/or deafness in an Italian family, Diabetic Medicine, vol.56, issue.4, pp.334-340, 2001.
DOI : 10.1023/A:1022685929755

J. Salles, T. Kasamatsu, S. Dib, and R. Moisés, ??-Cell Function in Individuals Carrying the Mitochondrial tRNA Leu (UUR) Mutation, Pancreas, vol.34, issue.1, pp.133-140, 2007.
DOI : 10.1097/01.mpa.0000246659.38375.4d

M. Sano, M. Ozawa, S. Shiota, Y. Momose, M. Uchigata et al., The T-C(8356) mitochondrial DNA mutation in a Japanese family, Journal of Neurology, vol.1, issue.6, pp.441-445, 1996.
DOI : 10.1007/BF00900496

E. Souied, J. Kaplan, G. Coscas, and G. Soubrane, Les dystrophies maculaires, Journal Français d'Ophtalmologie. sept, vol.26, issue.7, pp.743-62, 2003.

E. Souied, M. Salès, G. Soubrane, G. Coscas, B. Bigorie et al., Macular dystrophy, diabetes, and deafness associated with a large mitochondrial dma deletion, American Journal of Ophthalmology, vol.125, issue.1, pp.100-103, 1998.
DOI : 10.1016/S0002-9394(99)80243-8

D. Sternberg, E. Chatzoglou, P. Laforêt, G. Fayet, C. Jardel et al., Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders, Brain, vol.124, issue.5, pp.984-94, 2001.
DOI : 10.1093/brain/124.5.984

S. Suzuki, Y. Hinokio, S. Hirai, M. Onoda, M. Matsumoto et al., Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNALEU(UUR) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS), Diabetologia, vol.147, issue.8, pp.818-843, 1994.
DOI : 10.1007/BF00404339

S. Suzuki, Y. Hinokio, S. Hirai, M. Onoda, M. Matsumoto et al., Diabetes With Mitochondrial Gene tRNALYS Mutation, Diabetes Care, vol.17, issue.12, pp.1428-1460, 1994.
DOI : 10.2337/diacare.17.12.1428

S. Suzuki, Y. Hinokio, M. Ohtomo, M. Hirai, A. Hirai et al., The effects of coenzyme Q 10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation, Diabetologia, vol.41, issue.5, pp.584-592, 1998.
DOI : 10.1007/s001250050950

Y. Suzuki, S. Suzuki, Y. Hinokio, M. Chiba, Y. Atsumi et al., Diabetes Associated With a Novel 3264 Mitochondrial tRNALeu(UUR) mutation, Diabetes Care, vol.20, issue.7, pp.1138-1178, 1997.
DOI : 10.2337/diacare.20.7.1138

Y. Suzuki, K. Tsukuda, Y. Atsumi, Y. Goto, K. Hosokawa et al., Clinical Picture of a Case of Diabetes With Mitochondrial tRNA Mutation at Position 3271, Diabetes Care, vol.19, issue.11, pp.1304-1309, 1996.
DOI : 10.2337/diacare.19.11.1304

Y. Suzuki, M. Taniyama, A. Shimada, Y. Atumi, K. Matsuoka et al., GAD Antibody in Mitochondrial Diabetes Associated With tRNA(UUR) Mutation at Position 3271, Diabetes Care, vol.25, issue.6, pp.1097-1105, 2002.
DOI : 10.2337/diacare.25.6.1097

M. Tabebi, E. Mkaouar-rebai, M. Mnif, F. Kallabi, B. Mahmoud et al., A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with sever nephropathy, Biochemical and Biophysical Research Communications, vol.459, issue.3, pp.353-60, 2015.
DOI : 10.1016/j.bbrc.2015.01.151

M. Tawata, J. Hayashi, K. Isobe, E. Ohkubo, M. Ohtaka et al., A new mitochondrial DNA mutation at 14577 T/C is probably a major pathogenic mutation for maternally inherited type 2 diabetes, Diabetes, vol.49, issue.7, pp.1269-72, 2000.
DOI : 10.2337/diabetes.49.7.1269

F. Thomas, B. Balkau, F. Vauzelle-kervroedan, and L. Papoz, Maternal effect and familial aggregation in NIDDM. The CODIAB Study. CODIAB-INSERM-ZENECA Study Group, Diabetes, vol.43, issue.1, pp.63-70, 1994.
DOI : 10.2337/diabetes.43.1.63

V. Tiranti, C. P. Carella, F. Toscano, A. Soliveri, P. Girlanda et al., gene, Human Molecular Genetics, vol.4, issue.8, pp.1421-1428, 1995.
DOI : 10.1093/hmg/4.8.1421

K. Tsukuda, Y. Suzuki, K. Kameoka, N. Osawa, Y. Goto et al., Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNALeu(UUR) region, Diabetic Medicine, vol.14, issue.12, pp.1032-1039, 1997.
DOI : 10.1002/(SICI)1096-9136(199712)14:12<1032::AID-DIA504>3.0.CO;2-Y

J. Van-den-ouweland, H. Lemkes, W. Ruitenbeek, L. Sandkuijl, M. De-vijlder et al., Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness, Nature Genetics, vol.18, issue.5, pp.368-71, 1992.
DOI : 10.1016/0140-6736(91)90272-Q

J. Van-den-ouweland, H. Lemkes, R. Trembath, R. Ross, G. Velho et al., Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA Leu(UUR) gene, Diabetes, vol.43, issue.6, pp.746-51, 1994.
DOI : 10.2337/diab.43.6.746

G. Velho, M. Byrne, K. Clément, J. Sturis, M. Pueyo et al., Clinical Phenotypes, Insulin Secretion, and Insulin Sensitivity in Kindreds With Maternally Inherited Diabetes and Deafness Due to Mitochondrial tRNALeu(UUR) Gene Mutation, Diabetes, vol.45, issue.4, pp.478-87, 1996.
DOI : 10.2337/diab.45.4.478

B. Vialettes, V. Paquis-flucklinger, J. Pelissier, D. Bendahan, H. Narbonne et al., Phenotypic Expression of Diabetes Secondary to a T14709C Mutation of Mitochondrial DNA: Comparison with MIDD syndrome (A3243G mutation): a case report, Diabetes Care, vol.20, issue.11, pp.1731-1738, 1997.
DOI : 10.2337/diacare.20.11.1731

R. Whittaker, A. Schaefer, R. Mcfarland, R. Taylor, M. Walker et al., Prevalence and progression of diabetes in mitochondrial disease, Diabetologia, vol.85, issue.Suppl 1, pp.2085-2094, 2007.
DOI : 10.1007/s00125-007-0779-9

R. Whittaker, A. Schaefer, R. Mcfarland, R. Taylor, M. Walker et al., Diabetes and Deafness: Is it sufficient to screen for the mitochondrial 3243A>G mutation alone?, Diabetes Care, vol.30, issue.9, pp.2238-2247, 2007.
DOI : 10.2337/dc07-0466

T. Yamasoba, Y. Oka, K. Tsukuda, M. Nakamura, and K. Kaga, Gene, The Laryngoscope, vol.31, issue.1, pp.49-53, 1996.
DOI : 10.1097/00005537-199601000-00010

M. Zeviani, C. Gellera, C. Antozzi, M. Rimoldi, L. Morandi et al., Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR), The Lancet, vol.338, issue.8760, pp.143-150, 1991.
DOI : 10.1016/0140-6736(91)90136-D