Nyctalopin Expression in Retinal Bipolar Cells Restores Visual Function in a Mouse Model of Complete X-Linked Congenital Stationary Night Blindness

Mutations in the NYX gene that encodes the protein nyctalopin cause congenital stationary night blindness type 1. In no b-wave (nob) mice, a mutation in Nyx results in a functional phenotype that includes the absence of the electroretinogram b-wave and abnormal spontaneous and light-evoked activity...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Gregg, Ronald G., Kamermans, Maarten, Klooster, Jan, Lukasiewicz, Peter D., Peachey, Neal S., Vessey, Kirstan A., McCall, Maureen A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2933657/
https://ncbi.nlm.nih.gov/pubmed/17881478
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/jn.00608.2007
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados