A MELAS syndrome family harboring two mutations in mitochondrial genome

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a genetically heterogeneous mitochondrial disorder with variable clinical symptoms. Here, from the sequencing of the entire mitochondrial genome, we report a Korean MELAS family harboring two homopl...

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Detalhes bibliográficos
Main Authors: Choi, Byung-Ok, Hwang, Jung Hee, Kim, Joonki, Cho, Eun Min, Cho, Sun Young, Hwang, Su Jin, Lee, Hyang Woon, Kim, Song Ja, Chung, Ki Wha
Formato: Artigo
Idioma:Inglês
Publicado em: Korean Society of Medical Biochemistry and Molecular Biology 2008
Assuntos:
Short Communication
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2679288/
https://ncbi.nlm.nih.gov/pubmed/18587274
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3858/emm.2008.40.3.354
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