Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.

A human rhodopsin mutation, Gly-90-->Asp (Gly90Asp), cosegregated with an unusual trait of congenital nightblindness in 22 at-risk members of a large autosomal dominant kindred. Although rhodopsin mutations typically are associated with retinal degeneration, Gly90Asp-affected subjects up to age 3...

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Bibliografski detalji
Glavni autori: Sieving, P A, Richards, J E, Naarendorp, F, Bingham, E L, Scott, K, Alpern, M
Format: Artigo
Jezik:Inglês
Izdano: 1995
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC42724/
https://ncbi.nlm.nih.gov/pubmed/7846071
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