Human Genome Epidemiology Literature Finder
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Query Trace: Eye Diseases and ALMS1[original query] |
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ALMS1 null mutations: a common cause of Leber congenital amaurosis and early-onset severe cone-rod dystrophy. Clinical genetics 2015 May . Xu Y, Guan L, Xiao X, Zhang J, Li S, Jiang H, Jia X, Yin Y, Guo X, Wang J, Zhang |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
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