Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa

Benzer Materyaller

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