The autosomal recessive variety of congenital stationary night-blindness with myopia.

Samankaltaisia teoksia

• GNAT1 Associated with Autosomal Recessive Congenital Stationary Night Blindness
  Tekijä: Naeem, Muhammad Asif, et al.
  Julkaistu: (2012)
• A Naturally Occurring Canine Model of Autosomal Recessive Congenital Stationary Night Blindness
  Tekijä: Kondo, Mineo, et al.
  Julkaistu: (2015)
• TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness
  Tekijä: Audo, Isabelle, et al.
  Julkaistu: (2009)
• A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness
  Tekijä: Riazuddin, S. Amer, et al.
  Julkaistu: (2010)
• Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness
  Tekijä: Vincent, Ajoy, et al.
  Julkaistu: (2016)