Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r)

Antzeko izenburuak

• Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin.
  nork: Khaliq, S, et al.
  Argitaratua: (1999)
• Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32
  nork: Bessant, D., et al.
  Argitaratua: (1999)
• A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32.
  nork: Bessant, D A, et al.
  Argitaratua: (1998)
• Mutation analysis of GABRR1 and GABRR2 in autosomal recessive retinitis pigmentosa (RP25)
  nork: MARCOS, I, et al.
  Argitaratua: (2000)
• RP1 mutations cause autosomal recessive retinitis pigmentosa
  Argitaratua: (2005)