Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation

Mutations in TRPM1 are found in humans with an autosomal recessive form of complete congenital stationary night blindness (cCSNB). The Trpm1(−/−) mouse has been an important animal model for this condition. Here we report a new mouse mutant, tvrm27, identified in a chemical mutagenesis screen. Genet...

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Main Authors: Peachey, Neal S., Pearring, Jillian N., Bojang, Pasano, Hirschtritt, Matthew E., Sturgill-Short, Gwen, Ray, Thomas A., Furukawa, Takahisa, Koike, Chieko, Goldberg, Andrew F. X., Shen, Yin, McCall, Maureen A., Nawy, Scott, Nishina, Patsy M., Gregg, Ronald G.
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2012
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3545183/
https://ncbi.nlm.nih.gov/pubmed/22896717
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/jn.00137.2012
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