Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa

Podobné jednotky

• RP1 mutations cause autosomal recessive retinitis pigmentosa
  Vydáno: (2005)
• Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin.
  Autor: Khaliq, S, a další
  Vydáno: (1999)
• Evidence of RPGRIP1 gene mutations associated with recessive cone-rod dystrophy
  Autor: Hameed, A, a další
  Vydáno: (2003)
• Mutation analysis of GABRR1 and GABRR2 in autosomal recessive retinitis pigmentosa (RP25)
  Autor: MARCOS, I, a další
  Vydáno: (2000)
• Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigmentosa in an Indonesian family
  Autor: Siemiatkowska, Anna M., a další
  Vydáno: (2012)