Congenital stationary night blindness associated with mutations in GRM6 encoding glutamate receptor MGluR6

Br J Ophthalmol. 2006 May;90(5):653-4. doi: 10.1136/bjo.2005.086678.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Codon, Nonsense*
  • Female
  • Humans
  • Night Blindness / genetics*
  • Receptors, Metabotropic Glutamate / genetics*

Substances

  • Codon, Nonsense
  • Receptors, Metabotropic Glutamate
  • metabotropic glutamate receptor 6