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Article

The retinitis pigmentosa GTPase regulator (RPGR)- interacting protein: subserving RPGR function and participating in disk morphogenesis.

Proceedings of the National Academy of Sciences of the United States of America - 1 Apr 2003

Zhao Yun, Hong Dong-Hyun, Pawlyk Basil, Yue Guohua, Adamian Michael, Grynberg Marcin, Godzik Adam, Li Tiansen

Abstract excerpt

Retinitis pigmentosa is a photoreceptor degenerative disease leading to blindness in adulthood. Leber congenital amaurosis (LCA) describes a more severe condition with visual deficit in early childhood. Defects in the retinitis pigmentosa GTPase regulator (RPGR) and an RPGR-interacting protein (RPGRIP) are known causes of retinitis pigmentosa and LCA, respectively. Both proteins localize in the photoreceptor...

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Source

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Identifiers

PMID: 12651948
DOI: 10.1073/pnas.0637349100
PMCID: PMC153031

Genes

RPGR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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