Profiling the Mitochondrial Proteome of Leber’s Hereditary Optic Neuropathy (LHON) in Thailand: Down-Regulation of Bioenergetics and Mitochondrial Protein Quality Control Pathways in Fibroblasts with the 11778G>A Mutation

Leber’s Hereditary Optic Neuropathy (LHON) is one of the commonest mitochondrial diseases. It causes total blindness, and predominantly affects young males. For the disease to develop, it is necessary for an individual to carry one of the primary mtDNA mutations 11778G>A, 14484T>C or 3460G>...

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Main Authors: Tun, Aung Win, Chaiyarit, Sakdithep, Kaewsutthi, Supannee, Katanyoo, Wanphen, Chuenkongkaew, Wanicha, Kuwano, Masayoshi, Tomonaga, Takeshi, Peerapittayamongkol, Chayanon, Thongboonkerd, Visith, Lertrit, Patcharee
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4162555/
https://ncbi.nlm.nih.gov/pubmed/25215595
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0106779
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