Standardised measures of retinal function pinpoint genotype in X linked congenital stationary night blindness

Samankaltaisia teoksia

• Genotype-phenotype correlation in British families with X linked congenital stationary night blindness
  Tekijä: Allen, L E, et al.
  Julkaistu: (2003)
• Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.
  Tekijä: Boycott, K M, et al.
  Julkaistu: (1998)
• Nyctalopin Expression in Retinal Bipolar Cells Restores Visual Function in a Mouse Model of Complete X-Linked Congenital Stationary Night Blindness
  Tekijä: Gregg, Ronald G., et al.
  Julkaistu: (2007)
• Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: demonstration of homozygosity.
  Tekijä: Bech-Hansen, N T, et al.
  Julkaistu: (1993)
• Two Novel NYX Gene Mutations in the Chinese Families with X-linked Congenital Stationary Night Blindness
  Tekijä: Dai, Shuzhen, et al.
  Julkaistu: (2015)