Prevalence of maternally inherited diabetes and deafness in diabetic populations in the Netherlands
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF00418385.pdf
Reference6 articles.
1. van den Ouweland JMW, Lemkes HHPJ, Ruitenbeek W et al. (1992) Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nature Genetics 1: 368?371
2. Katagiri H, Asano T, Ishihara H et al. (1994) Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNALeu(UUR) gene mutation in Japanese patients. Diabetologia 37: 504?510
3. Kadowaki T, Kadowaki H, Mori Y et al. (1994) A subtype of diabetes mellitus associated with a mutation in the mitochondrial gene. N Eng J Med 330: 962?968
4. van den Ouweland JMW, Lemkes HHPJ, Trembath RC et al. (1994) Maternally inherited diabetes and deafness (MIDD) is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNALeu(UUR) gene. Diabetes 43: 746?751
5. Vionnet N, Passa P, Froguel P (1993) Prevalence of mitochondrial gene mutations in families with diabetes mellitus. Lancet 342: 1429?1430
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