Mapping of the human cone transducin α-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt disease

This publication has 14 references indexed in Scilit:

• A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1
  Nature Genetics, 1993
• Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partner.
  Molecular and Cellular Biology, 1993
• Characterization of the Gene Encoding Human Cone Transducin α-Subunit (GNAT2)
  Genomics, 1993
• Recessive mutations in the gene encoding the β–subunit of rod phosphodiesterase in patients with retinitis pigmentosa
  Nature Genetics, 1993
• Detection of point mutations in the p53 gene: Comparison of single-strand conformation polymorphism, constant denaturant gel electrophoresis, and hydroxylamine and osmium tetroxide techniques
  Human Mutation, 1993
• Transgenic mice with a rhodopsin mutation (Pro23His): A mouse model of autosomal dominant retinitis pigmentosa
  Neuron, 1992
• Rhodopsin and autosomal dominant retinitis pigmentosa
  Eye, 1992
• High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid Clones
  Science, 1990
• Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
  Genomics, 1989
• Chromosomal localization of genes encoding guanine nucleotide-binding protein subunits in mouse and human.
  Proceedings of the National Academy of Sciences, 1988