Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa.
Year: 2000
Type: article
Study design: Observational Study
Source: PubMed
Institution: University of Pennsylvania
Language: English
Subfield: Ophthalmology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
Funder: National Eye Institute
OpenAlex ID: W1581865425
