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Results 1 - 3 of 3 for Incomplete congenital stationary night blindness
  1. Autosomal recessive congenital stationary night blindness 
    ... recessive complete congenital stationary night blindness Autosomal recessive incomplete congenital stationary night blindness Genetic Testing Registry: Cone-rod synaptic disorder, congenital ...
    https://medlineplus.gov/...ive-congenital-stationary-night-blindness - Genetics
  2. X-linked congenital stationary night blindness 
    ... channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness. Nat Genet. 1998 Jul;19(3):264-7. ... Bech-Hansen NT. Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F. Can J ...
    https://medlineplus.gov/...ked-congenital-stationary-night-blindness - Genetics
  3. CACNA1F gene 
    ... channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness. Nat Genet. 1998 Jul;19(3):264-7. ... 20 CACNA1F mutations identified in 36 families with incomplete X-linked ... night blindness, and characterization of splice variants. Hum Genet. 2001 ...
    https://medlineplus.gov/genetics/gene/cacna1f - Genetics