Work

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness

Year: 1993

Type: article

Study design: Case Report

Source: Nature Genetics

DOI: 10.1038/ng0793-280

Authors: Thaddeus P. Dryja, Eliot L. Berson, Vikram R. Rao, Daniel D. Oprian

Institutions: Harvard University, Brandeis University

Language: English

Topic: Retinal Development and Disorders

Subfield: Ophthalmology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: National Eye Institute

Awards: CANDIDATE GENE STUDY OF INHERITED RETINAL DEGENERATIONS, G6413170261, Structure-Function Studies of Rhodopsin

OpenAlex ID: W1994104925

FWCI: 38.54

Cites: 25

Cited by: 341

Related to: 10