Work

The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa.

Year: 2007

Type: article

Study design: Observational Study

Source: PubMed

Authors: Anisa I Gire, Lori S Sullivan, Sara J Bowne, David G Birch, Dianna Hughbanks-Wheaton, John R Heckenlively, Stephen P Daiger

Institutions: The University of Texas Health Science Center at Houston, Retina Foundation of the Southwest

Language: English

Topic: Retinal Development and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: National Eye Institute

Awards: DNA Linkage Studies of Degenerative Retinal Diseases, Retinal Pathophysiology of Infants and Adults

OpenAlex ID: W40817687

FWCI: 1.588

Cites:

Cited by: 56

Related to: 10