Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy-Reference-Cited by-同舟云学术

Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy

Published:2020-09 Issue:38 Volume:295 Page:13224-13238
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Ji Yanchun,Zhang Juanjuan,Lu Yuanyuan,Yi Qiuzi^ORCID,Chen Mengquan,Xie Shipeng,Mao Xiaoting,Xiao Yun,Meng Feilong,Zhang Minglian,Yang Rulai,Guan Min-Xin^ORCID

Funder

National Natural Science Foundation of China

MOST | National Key Research and Development Program of China

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference81 articles.

1. Leber hereditary optic neuropathy: exemplar of an mtDNA disease;Wallace;Handb. Exp. Pharmacol.,2017

2. Leber's hereditary optic neuropathy;Newman;Ophthalmol. Clin. N. Am,1993

3. Clinical picture of LHON;Nikoskelainen;Clin. Neurosci.,1994

4. Leber's hereditary optic neuropathy;Sadun;Curr. Treat Options Neurol,2011

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

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