Identification of genes causing photoreceptor degenerations leading to blindness

This publication has 83 references indexed in Scilit:

• Rhodopsin mutations in inherited retinal dystrophies and dysfunctions
  Progress in Retinal and Eye Research, 1997
• Novel rhodopsin mutation (M216R) in a Danish family with autosomal dominant retinitis pigmentosa
  Ophthalmic Genetics, 1996
• Missense rhodopsin mutation in a family with recessive RP
  Nature Genetics, 1994
• Retinitis pigmentosa in Southern Africa
  Clinical Genetics, 1993
• A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa
  Nature Genetics, 1992
• A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
  Nature, 1990
• Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3
  Genomics, 1989
• Retinitis pigmentosa
  Survey of Ophthalmology, 1988
• Assignment of the rhodopsin gene to human chromosome three, region 3q21–3q24 byin situhybridization studies
  Current Eye Research, 1986
• Isolation and nucleotide sequence of the gene encoding human rhodopsin.
  Proceedings of the National Academy of Sciences, 1984