Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese families-Reference-Cited by-同舟云学术

Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese families

Published:2014-09 Issue: Volume:18 Page:18-26
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Zhang Juanjuan,Jiang Pingping,Jin Xiaofen,Liu Xiaoling,Zhang Minglian,Xie Shipeng,Gao Min,Zhang Sai,Sun Yan-Hong,Zhu Jinping,Ji Yanchun,Wei Qi-Ping,Tong Yi,Guan Min-Xin

Funder

Ministry of Science and Technology of the People's Republic of China

Natural Science Foundation of China

Ministry of Science and Technology of Zhejiang Province

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference53 articles.

1. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA;Andrews;Nat. Genet.,1999

2. Severe impairment of complex I-driven adenosine triphosphate synthesis in Leber hereditary optic neuropathy cybrids;Baracca;Arch. Neurol.,2005

3. Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines;Beretta;Brain,2004

4. Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy;Bi;Mol. Vis.,2012

5. Assaying mitochondrial respiratory complex activity in mitochondria isolated from human cells and tissues;Birch-Machin;Methods Cell Biol.,2001

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