4Gat-Yablonski G, Shalitin S, Phillip M. Maturity onset diabetes of the young--review. Pediatr Endocrinol Rev, 2006, 3 Suppl 3 : 514 - 520.
5Yamagata K, Furuta H, Oda N, et al. Mutations in the hepatocyte nuclear factor-4-alpha gene in maturity-onset diabetes of the young ( MODY1 ). Nature, 1996, 384:458-460.
6Njolstad PR, Sovik O, Cuesta-Munoz A, et al. Neonatal diabetes mellitus due to complete glucokinase deficiency. N Engl J Med, 2001, 344 : 1588-1592.
7Yamagata K, Oda N, Kaisaki PJ, et al. Mutations in the hepatocyte nuclear factor-1-alpha gene in maturity-onset diabetes of the young (MODY3). Nature, 1996, 384:455-458.
8Stoffers DA, Ferrer J, Clarke WL, et al. Early-onset type 2 diabetes mellitus ( MODY4 ) linked to IPF1. Nat Genet, 1997, 17:138-139.
9Horikawa Y, lwasaki N, Hara M, et al. Mutations in hepatocyte nuclear factor 113 gene (TCF2) associated with MODY. Nat Genet, 1997, 17:384-385.
10Malecki MT, Jhala US, Antonellis A, et al. Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus. Nat Genet, 1999, 23:323-328.
3Nakamura S, Yoshinari M, Doi Y, et al. Renal complications in patients with diabetes mellitus associated with an A to G mutation of mitochondrial DNA at the 3243 position of leucine Trna[J]. Diabetes Res Clin Pract, 1999,44:183-189.
4Ballinger S, Shoffner J, Hedaya E, et al. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion[J]. Nat Genet, 1992,1:11-15.
5Mkaouar-Rebai E, Chamkha I, Kammoun T, et al. A novel MT- CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial C OI/tRNA (Ser(UCN))genes in a patient with hearing impairment, diabetes and congenital visual loss[J]. Biochem Biophys Res Commun,2013,430:585-591.
6Mezghani N, Mnif M, Mkaouar-Rebai E, et al. A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions[J]. Biochem Biophys Res Commun,2013,431:670-674.
7Guillausseau P, Massin P, Dubois-LaForgue D, et al. Maternally inherited diabetes and deafness: a muhicenter study[J]. Ann Intern Med,2001,134:721-728.
8Martikainen M, Ronnemaa T, Majamaa K, et al. Prevalence of mitochondrial diabetes in southwestern Finland: a molecular epidemiological study[J]. Acta Diabetol,2013,50:737-741.
9Wang S, Wu S, Zheng T, et al. Mitochondrial DNA mutations in diabetes mellitus patients in Chinese Han population[J]. Gene, 2013,531:472-475.
10Maassen J,'T Hart L, Van Essen E, et al. Mitochondrial diabetes: molecular mechanisms and clinical presentation[J]. Diabetes,2004,53 Suppl 1:S103-109.