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Paradoxical effect of sodium valproate that aggravates epilepsy of MELAS in a patient with A3243G mutation of the mitochondrial DNA

โœ Scribed by Chen, Yi-Min ;Lin, Chih-Ming ;Thajeb, Peterus


Book ID
111489749
Publisher
Walter de Gruyter GmbH
Year
2007
Tongue
English
Weight
326 KB
Volume
2
Category
Article
ISSN
2391-5463

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Maternally inherited cardiomyopathy: A n
โœ Gabriella Silvestri; Enrico Bertini; Serenella Servidei; Michele Rana; Elisabett ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 296 KB ๐Ÿ‘ 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