LCA9Leber congenital amaurosis 9Leber congenital amaurosis caused by mutation in NMNAT1Leber congenital amaurosis type 9NMNAT1 Leber congenital amaurosisamaurosis congenita of Leber, type 9
Definition
Any Leber congenital amaurosis in which the cause of the disease is a mutation in the NMNAT1 gene.
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