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Clinical features of MELAS and its relation with A3243G gene point mutation

Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) mostly occur in children. The point mutation A3243G of mitochondrial DNA (mtDNA) may work as a specific bio-marker for mitochondrial disorders. The related clinical features, however, may vary among individuals. This...

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Detalhes bibliográficos
Publicado no:Int J Clin Exp Pathol
Main Authors: Zhang, Jin, Guo, Junhong, Fang, Wanghui, Jun, Qili, Shi, Kaili
Formato: Artigo
Idioma:Inglês
Publicado em: e-Century Publishing Corporation 2015
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4680494/
https://ncbi.nlm.nih.gov/pubmed/26722549
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