Response from the author
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF02743280.pdf
Reference13 articles.
1. Dorner G, Mohnike A, Steindel E (1975) On possible genetic and epigenetic modes of diabetic transmission. Endokrinologie 66: 225–227
2. Ballinger SW, Shoffner JM, Hedaya EV et al. (1992) Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion. Nature Genetics 1: 11–15
3. 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 and deafness. Nature Genetics 1: 368–371
4. Reardon W, Ross RJW, Sweeney MG et al. (1992) Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA. Lancet 340: 1376–1379
5. Obermaier-Kusser B, Paetzke-Brunner I, Enter C et al. (1991) Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome (tRNALeu (UUR)). FEBS Lett 286: 67–70
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1. Association between HLA and islet cell antibodies in diabetic patients with a mitochondrial DNA mutation at base pair 3243;Diabetologia;1996-10
2. The genes influencing the susceptibility to IDDM in humans;Journal of Endocrinological Investigation;1994-07
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