Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families-Reference-Cited by-同舟云学术

Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families

Published:2013-11 Issue:6 Volume:13 Page:772-781
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Zhang Juanjuan,Zhao Fuxin,Fu Qun,Liang Min,Tong Yi,Liu Xiaoling,Lin Bei,Mi Hui,Zhang Minglian,Wei Qi-Ping,Xue Ling,Jiang Pingping,Zhou Xiangtian,Mo Jun Qin,Huang Taosheng,Qu Jia,Guan Min-Xin

Funder

National Natural Science Foundation of China

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

Key Technologies Research and Development Program

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

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4. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations;Brown;Hum. Mutat.,1995

5. Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation;Brown;J. Biol. Chem.,2000

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