Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa

This publication has 8 references indexed in Scilit:

• Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa
  Genomics, 1993
• A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea.
  Human Molecular Genetics, 1993
• Butterfly–shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene
  Nature Genetics, 1993
• Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy
  Nature Genetics, 1993
• A medley of retinal dystrophies
  Nature Genetics, 1993
• A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa
  Nature, 1991
• Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa
  Nature, 1991
• The human retinal degeneration slow (RDS) gene: Chromosome assignment and structure of the mRNA
  Genomics, 1991