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...

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Main Authors: Gregg, Ronald G., Kamermans, Maarten, Klooster, Jan, Lukasiewicz, Peter D., Peachey, Neal S., Vessey, Kirstan A., McCall, Maureen A.
Format: Artigo
Jezik:Inglês
Izdano: 2007
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Article
Online dostop: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
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