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A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene (MTCYB) in a Patient With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes Syndrome

✍ Scribed by Emmanuele, V.; Sotiriou, E.; Rios, P. G.; Ganesh, J.; Ichord, R.; Foley, A. R.; Akman, H. O.; DiMauro, S.

Book ID: 126904989
Publisher: SAGE Publications
Year: 2012
Tongue: English
Weight: 402 KB
Volume: 28
Category: Article
ISSN: 0883-0738
DOI: 10.1177/0883073812445787

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