Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration
出版年份 2012 全文链接
标题
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration
作者
关键词
-
出版物
NATURE GENETICS
Volume 44, Issue 9, Pages 1035-1039
出版商
Springer Nature
发表日期
2012-07-30
DOI
10.1038/ng.2356
参考文献
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