Abnormal activation and inactivation mechanisms of rod transduction in patients with autosomal dominant retinitis pigmentosa and the pro-23-his mutation.
Year: 1995
Type: article
Source: PubMed
Authors: D G Birch, D C Hood, S Nusinowitz, D R Pepperberg
Institution: Retina Foundation of the Southwest
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
Funder: National Institutes of Health
OpenAlex ID: W1600673266
