Congenital stationary night blindness 1G

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

Also known as: CSNB1G, congenital stationary night blindness type 1G, night blindness, congenital stationary, type 1G

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