Novel Dominant Rhodopsin Mutation Triggers Two Mechanisms of Retinal Degeneration and Photoreceptor Desensitization

A variety of rod opsin mutations result in autosomal dominant retinitis pigmentosa and congenital night blindness in humans. One subset of these mutations encodes constitutively active forms of the rod opsin protein. Some of these dominant rod opsin mutant proteins, which desensitize transgenic Xeno...

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Bibliografiska uppgifter
I publikationen:J Neurosci
Huvudupphovsmän: Iakhine, Roustem, Chorna-Ornan, Irit, Zars, Troy, Elia, Natalie, Cheng, Yan, Selinger, Zvi, Minke, Baruch, Hyde, David R.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Society for Neuroscience 2004
Ämnen:
Neurobiology of Disease
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6729501/
https://ncbi.nlm.nih.gov/pubmed/15014127
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.5426-03.2004
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