A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens
Year: 1993
Type: article
Source: Nature Genetics
DOI: 10.1038/ng0393-208
Institutions: Massachusetts Eye and Ear Infirmary, Harvard University
Language: English
Subfield: Ophthalmology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
Funder: National Eye Institute
OpenAlex ID: W1980805294
