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The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation

✍ Scribed by S. Suzuki; Y. Hinokio; M. Ohtomo; M. Hirai; A. Hirai; M. Chiba; S. Kasuga; Y. Satoh; H. Akai; T. Toyota


Publisher
Springer
Year
1998
Tongue
English
Weight
191 KB
Volume
41
Category
Article
ISSN
0012-186X

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Maternally inherited cardiomyopathy: A n
✍ Gabriella Silvestri; Enrico Bertini; Serenella Servidei; Michele Rana; Elisabett πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 296 KB πŸ‘ 2 views

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