[TRPM1, a new gene implicated in congenital stationary night blindness]

Med Sci (Paris). 2010 Mar;26(3):241-4. doi: 10.1051/medsci/2010263241.
[Article in French]
No abstract available

MeSH terms

  • Calcium / metabolism
  • Calcium-Binding Proteins / genetics
  • Codon, Nonsense
  • Genes, Recessive
  • Humans
  • Models, Genetic
  • Mutation
  • Night Blindness / congenital
  • Night Blindness / genetics*
  • Phenotype
  • Signal Transduction
  • TRPM Cation Channels / genetics*

Substances

  • CABP4 protein, human
  • Calcium-Binding Proteins
  • Codon, Nonsense
  • TRPM Cation Channels
  • TRPM1 protein, human
  • Calcium