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Article

The retinitis pigmentosa protein RP2 interacts with polycystin 2 and regulates cilia-mediated vertebrate development.

Human molecular genetics - 15 Nov 2010

Hurd Toby, Zhou Weibin, Jenkins Paul, Liu Chia-Jen, Swaroop Anand, Khanna Hemant, Martens Jeffrey, Hildebrandt Friedhelm, Margolis Ben

Abstract excerpt

Ciliopathies represent a growing group of human genetic diseases whose etiology lies in defects in ciliogenesis or ciliary function. Given the established entity of renal-retinal ciliopathies, we have been examining the role of cilia-localized proteins mutated in retinitis pigmentosa (RP) in regu...

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Identifiers

PMID: 20729296
DOI: 10.1093/hmg/ddq355
PMCID: PMC2957320

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20729296-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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