(Q32140436)
English
congenital stationary night blindness 1G
congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in homozygous mutation in the GNAT1 gene on chromosome 3p21
- CSNB1G
- congenital stationary night blindness type 1G
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G; CSNB1G
Statements
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference