A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

This publication has 13 references indexed in Scilit:

• De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis
  Nature Genetics, 1998
• Human bZIP Transcription Factor GeneNRL:Structure, Genomic Sequence, and Fine Linkage Mapping at 14q11.2 and Negative Mutation Analysis in Patients with Retinal Degeneration
  Genomics, 1997
• Retinopathy induced in mice by targeted disruption of the rhodopsin gene
  Nature Genetics, 1997
• The bZIP Transcription Factor Nrl Stimulates Rhodopsin Promoter Activity in Primary Retinal Cell Cultures
  Published by Elsevier ,1996
• The basic motif-leucine zipper transcription factor Nrl can positively regulate rhodopsin gene expression.
  Proceedings of the National Academy of Sciences, 1996
• Retinal Photoreceptor Dystrophies LI. Edward Jackson Memorial Lecture
  American Journal of Ophthalmology, 1995
• Transgenic mice with a rhodopsin mutation (Pro23His): A mouse model of autosomal dominant retinitis pigmentosa
  Neuron, 1992
• A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis piamentosa
  Human Molecular Genetics, 1992
• A conserved retina-specific gene encodes a basic motif/leucine zipper domain.
  Proceedings of the National Academy of Sciences, 1992
• Rapid detection of single base mismatches as heteroduplexes on Hydrolink gels
  Trends in Genetics, 1991