Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosa

This publication has 12 references indexed in Scilit:

• Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa
  Genomics, 1991
• Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa.
  Proceedings of the National Academy of Sciences, 1991
• Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresis.
  1991
• Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site
  Genomics, 1991
• Rhodopsin mutations in autosomal dominant retinitis pigmentosa.
  Proceedings of the National Academy of Sciences, 1991
• A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa.
  1991
• Mutations within the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa
  New England Journal of Medicine, 1990
• A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
  Nature, 1990
• Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
  Genomics, 1989
• Regulation of transmembrane signaling by receptor phosphorylation
  Cell, 1987