A recurrent deletion mutation in OPA1 causes autosomal...

Scientific Reports 2015 / 5 Vol. 4; Iss. 1

A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family

Zhang, Liping, Shi, Wei, Song, Liming, Zhang, Xiao, Cheng, Lulu, Wang, Yanfang, Ge, Xianglian, Li, Wei, Zhang, Wei, Min, Qingjie, Jin, Zi-Bing, Qu, Jia, Gu, Feng
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Volume:
4
Language:
english
Journal:
Scientific Reports
DOI:
10.1038/srep06936
Date:
May, 2015
File:
PDF, 3.57 MB
english, 2015
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