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Diabetes Research and Clinical Practice
Volume 59, Issue 3
, Pages 207-217
, March 2003
Clinical features of diabetes mellitus with the mitochondrial DNA 3243 (A–G) mutation in Japanese: Maternal inheritance and mitochondria-related complications
References
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Ministry of Health and Welfare, Japan, Kokumin Eiyou no Genjou 1996 (Report of National Nutrition Survey), Daiichi Shuppan Co, Tokyo, 1998 (in Japanese).
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Importance of maternal history of non-insulin dependent diabetic patients.
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Maternal inherited diabetes is predominant in Japanese and has influence on sibling.
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Optic neuropathy associated with mitochondrial tRNA[Leu(UUR)] A3243G mutation.
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- . Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease. J. Hum. Genet. 2001;46:330–334
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- . Molecular and histological evaluation of pancreata from patients with a mitochondrial gene mutation associated with impaired insulin secretion. Biochem. Biophys. Res. Commun. 1999;259:149–156
PII: S0168-8227(02)00246-2
© 2002 Elsevier Science Ireland Ltd. All rights reserved.
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Diabetes Research and Clinical Practice
Volume 59, Issue 3
, Pages 207-217
, March 2003
