Congenital stationary night blindness autosomal dominant 3

A congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the GNAT1 gene on chromosome 3p21.

Also known as: CSNBAD3, congenital stationary night blindness autosomal dominant type 3, night blindness, congenital stationary, autosomal dominant type 3, night blindness, congenital stationary, Nougaret type, night blindness, congenital stationary, autosomal dominant 3

36 clinical trials for this condition and its sub-types.