Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients

BACKGROUND: Leber hereditary optic neuropathy (LHON) is a mitochondrial disorder with gender biased and incomplete penetrance. The majority of LHON patients are caused by one of the three primary mutations (m.3460G > A, m.11778G > A and m.14484T > C). Rare pathogenic mutations have been occ...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux: Zhang, A-Mei, Jia, Xiaoyun, Guo, Xiangming, Zhang, Qingjiong, Yao, Yong-Gang
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2012
Sujets:
Research
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3372436/
https://ncbi.nlm.nih.gov/pubmed/22400981
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-5876-10-43
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires