Leber’s hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation-Reference-Cited by-同舟云学术

Leber’s hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation

Published:2009-11 Issue:3 Volume:389 Page:466-472
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Zhao Fuxin,Guan Minqiang,Zhou Xiangtian,Yuan Meixia,Liang Ming,Liu Qi,Liu Yan,Zhang Yongmei,Yang Li,Tong Yi,Wei Qi-Ping,Sun Yan-Hong,Qu Jia,Guan Min-Xin

Funder

National Institute on Deafness and Other Communication Disorders

National Science Foundation of China

Zhejiang Provincial Natural Science Foundation of China

Zhejiang Province, China

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference34 articles.

1. Leber’s hereditary optic neuropathy;Newman;Ophthalmol. Clin. North Am.,1993

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

3. Leber hereditary optic neuropathy;Man;J. Med. Genet.,2002

4. Mitochondrial DNA mutation associated with Leber’s hereditary optic neuropathy;Wallace;Science,1988

5. LHON and other optic nerve atrophies: the mitochondrial connection;Howell;Dev. Ophthalmol.,2003

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