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Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis
Pei Wen Chiang, Juan Wang, Yang Chen, Quan Fu, Jing Zhong, Yanhua Chen, Xin Yi, Renhua Wu, Haixue Gan, Yong Shi, Yanling Chen, Christopher Barnett, Dianna Wheaton, Megan Day, Joanne Sutherland, Elise Heon, Richard G. Weleber, Luis Alexandre Rassi Gabriel, Peikuan Cong, Kuanghsiang Chuang
Research output: Contribution to journal › Article › peer-review
108
Scopus
citations