Exome sequencing identifies NMNAT1 mutations as a cause of...

Nature Genetics 2012 / 7 Vol. 44; Iss. 9

Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis

Chiang, Pei-Wen, Wang, Juan, Chen, Yang, Fu, Quan, Zhong, Jing, Chen, Yanhua, Yi, Xin, Wu, Renhua, Gan, Haixue, Shi, Yong, Chen, Yanling, Barnett, Christopher, Wheaton, Dianna, Day, Megan, Sutherland,
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Volume:
44
Language:
english
Journal:
Nature Genetics
DOI:
10.1038/ng.2370
Date:
July, 2012
File:
PDF, 217 KB
english, 2012
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