(Q32144035)

English

congenital stationary night blindness 1H

congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the GNB3 gene on chromosome 12p13

  • CSNB1H
  • congenital stationary night blindness type 1H
  • Night Blindness, Congenital Stationary, Type 1H
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