Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis
Nature Genetics2012Vol. 44(9), pp. 972–974
Citations Over TimeTop 10% of 2012 papers
Pei-Wen Chiang, Juan Wang, Yang Chen, Quan Fu, Jing Zhong, Yanhua Chen, Xin Yi, Renhua Wu, Haixue Gan, Yongyong Shi, Yanling Chen, Christopher Barnett, Dianna K. Wheaton, Megan A Day, Joanne Sutherland, Elise Héon, Richard G. Weleber, Luís Alexandre Rassi Gabriel, Peikuan Cong, Kuang‐Hsiang Chuang, Sheng Ye, Juliana Maria Ferraz Sallum, Ming Qi
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