Associated Papers
NYX mutations in four families with high myopia with or without CSNB1.
Zhou L et al.
Molecular Vision, 2015
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.
Zeitz C et al.
American Journal of Human Genetics, 2013
Mutations in NYX of individuals with high myopia, but without night blindness.
Zhang Q et al.
Molecular Vision, 2007
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