Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies

Samankaltaisia teoksia

• Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies
  Tekijä: Payne, A., et al.
  Julkaistu: (1999)
• GUCY2D mutations in retinal guanylyl cyclase 1 provide biochemical reasons for dominant cone–rod dystrophy but not for stationary night blindness
  Tekijä: Peshenko, Igor V., et al.
  Julkaistu: (2021)
• Reanalysis of Association of Pro50Leu Substitution in Guanylate Cyclase Activating Protein-1 With Dominant Retinal Dystrophy
  Tekijä: Mahroo, Omar A., et al.
  Julkaistu: (2020)
• The Function of Guanylate Cyclase 1 and Guanylate Cyclase 2 in Rod and Cone Photoreceptors
  Tekijä: Baehr, Wolfgang, et al.
  Julkaistu: (2007)
• Mutation analysis at codon 838 of the Guanylate Cyclase 2D gene in Spanish families with autosomal dominant cone, cone-rod, and macular dystrophies
  Tekijä: Garcia-Hoyos, Maria, et al.
  Julkaistu: (2011)