Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6

Gelijkaardige items

• Congenital stationary night blindness associated with mutations in GRM6 encoding glutamate receptor MGluR6
  door: O'Connor, E, et al.
  Gepubliceerd in: (2006)
• Low prevalence of LRAT mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa
  door: Sweeney, Meredith O., et al.
  Gepubliceerd in: (2007)
• Disease Course in Patients with Autosomal Recessive Retinitis Pigmentosa due to the USH2A Gene
  door: Sandberg, Michael A., et al.
  Gepubliceerd in: (2008)
• A missense mutation in Grm6 reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function
  door: Peachey, Neal S., et al.
  Gepubliceerd in: (2017)
• Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa
  door: McGee, Terri L., et al.
  Gepubliceerd in: (2010)