Mutations in the RP2 Gene Cause Disease in 10% of Families with Familial X-Linked Retinitis Pigmentosa Assessed in This Study

This publication has 11 references indexed in Scilit:

• Positional cloning of the gene for X-linked retinitis pigmentosa 2
  Nature Genetics, 1998
• Spectrum of Mutations in the RPGR Gene That Are Identified in 20% of Families with X-Linked Retinitis Pigmentosa
  American Journal of Human Genetics, 1997
• Mapping the RP2 locus for X-linked retinitis pigmentosa on proximal Xp: a genetically defined 5-cM critical region and exclusion of candidate genes by physical mapping.
  Genome Research, 1996
• Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1
  Human Molecular Genetics, 1996
• Pathway Leading to Correctly Folded β-Tubulin
  Cell, 1996
• A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3)
  Nature Genetics, 1996
• Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests.
  Proceedings of the National Academy of Sciences, 1990
• Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.
  Proceedings of the National Academy of Sciences, 1989
• Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28
  Nature, 1984
• X-linked retinitis pigmentosa.
  British Journal of Ophthalmology, 1975