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Results 1 - 3 of 3 for Nystagmus "1," "congenital," "X-linked"
  1. FRMD7 gene 
    ... newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus. Nat Genet. 2006 Nov;38(11):1242-4. doi: 10.1038/ng1893. Epub 2006 Oct 1. Erratum In: Nat Genet. 2011 Jul;43(7): ...
    https://medlineplus.gov/genetics/gene/frmd7 - Genetics
  2. CACNA1F gene 
    ... disc atrophy alters the structure of the alpha-1 subunit, which probably leads to the production of nonfunctional CaV1.4 channels. This mutation has also been identified in at least one Japanese family with X-linked congenital stationary night blindness. It is unclear why this ...
    https://medlineplus.gov/genetics/gene/cacna1f - Genetics
  3. NYX gene 
    ... NYX gene have been identified in people with X-linked congenital stationary night ... movements of the eyes (nystagmus), and eyes that do not look in the ...
    https://medlineplus.gov/genetics/gene/nyx - Genetics