Leber's Hereditary Optic Neuropathy Is Associated with the T12338C Mutation in Mitochondrial ND5 Gene in Six Han Chinese Families-Reference-Cited by-同舟云学术

Leber's Hereditary Optic Neuropathy Is Associated with the T12338C Mutation in Mitochondrial ND5 Gene in Six Han Chinese Families

Published:2011-05 Issue:5 Volume:118 Page:978-985
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Liu Xiao-Ling,Zhou Xiangtian,Zhou Jian,Zhao Fuxin,Zhang Juanjuan,Li Chengwu,Ji Yanchun,Zhang Yu,Wei Qi-Ping,Sun Yan-Hong,Yang Li,Lin Bing,Yuan Yumin,Li Yingzi,Qu Jia,Guan Min-Xin

Publisher

Elsevier BV

Subject

Ophthalmology

Reference50 articles.

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2. Spectrum of mitochondrial DNA mutations in Leber's hereditary optic neuropathy;Brown;Clin Neurosci,1994

3. Inherited mitochondrial optic neuropathies;Yu-Wai-Man;J Med Genet,2009

4. Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders;Carelli;Biochim Biophys Acta,2009

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

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