(Q32144078)
English
congenital stationary night blindness 1E
congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the GPR179 gene on chromosome 17q12
- congenital stationary night blindness 1E autosomal recessive
- CSNB1E
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E; CSNB1E
- congenital stationary night blindness type 1E
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E
- Csnb, Complete, Autosomal Recessive
Statements
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Identifiers
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