(Q32144004)
English
congenital stationary night blindness 1F
congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25
- CSNB1F
- congenital stationary night blindness 1F autosomal recessive
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F
- congenital stationary night blindness type 1F
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F; CSNB1F
Statements
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Identifiers
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1 reference