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Mitochondrial DNA mutation at np 3243 in a family with maternally inherited diabetes mellitus

✍ Scribed by L. Rigoli; D.C. Salpietro; R.A. Caruso; A. Chiarenza; I. Barberi


Publisher
Springer
Year
1999
Tongue
English
Weight
118 KB
Volume
36
Category
Article
ISSN
0940-5429

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Maternally inherited cardiomyopathy: A n
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The A to G transition at nt.3243 of the tRNA Leu(UUR) gene of mtDNA, commonly associated with MELAS, was detected in several members of a family affected by a maternally inherited form of hypertrophic cardiomyopathy. These findings suggest adding cardiomyopathy in the list of phenotypes associated w