The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial

This publication has 43 references indexed in Scilit:

• Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies
  European Journal of Human Genetics, 1998
• Long-term follow-up of stargardt’s disease and fundus flavimaculatus
  Ophthalmology, 1998
• Stargardt's ABCR is localized to the disc membrane of retinal rod outer segments
  Nature Genetics, 1997
• Correction: Corrigendum: A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy
  Nature Genetics, 1997
• The 220-kDa Rim Protein of Retinal Rod Outer Segments Is a Member of the ABC Transporter Superfamily
  Journal of Biological Chemistry, 1997
• Genetic fine mapping of the gene for recessive Stargardt disease
  Human Genetics, 1996
• Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
  Nature Genetics, 1995
• A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa
  Nature, 1991
• Light stimulates phosphorylation of two large membrane proteins in frog photoreceptors
  Biochemistry, 1985
• Über familiäre, progressive Degeneration in der Maculagegend des Auges
  Albrecht von Graefes Archiv für Ophthalmologie, 1909