Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa

Registos relacionados

• Mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa: high prevalence and phenotypic variation
  Por: Bernal, S, et al.
  Publicado em: (2003)
• Mutation Spectrum of EYS in Spanish Patients with Autosomal Recessive Retinitis Pigmentosa
  Por: Barragán, Isabel, et al.
  Publicado em: (2010)
• Molecular analysis of ABCA4 and CRB1 genes in a Spanish family segregating both Stargardt disease and autosomal recessive retinitis pigmentosa
  Por: Riveiro-Alvarez, Rosa, et al.
  Publicado em: (2008)
• Novel homozygous mutation in the alpha subunit of the rod cGMP gated channel (CNGA1) in two Spanish sibs affected with autosomal recessive retinitis pigmentosa
  Por: Paloma, E, et al.
  Publicado em: (2002)
• Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosa
  Por: Yang, Yin, et al.
  Publicado em: (2016)