(Q32144064)
English
congenital stationary night blindness 1D
congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in homozygous mutation in the SLC24A1 gene on chromosome 15q22
- congenital stationary night blindness 1D autosomal recessive
- CSNB1D
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D
- congenital stationary night blindness type 1D
- Csnb, Complete, Autosomal Recessive
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D; CSNB1D
Statements
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Identifiers
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