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Article

The ciliary protein Rpgrip1l in development and disease.

Developmental biology - 1 Oct 2018

Wiegering Antonia, Rüther Ulrich, Gerhardt Christoph

Abstract excerpt

RPGRIP1L is an evolutionary highly conserved gene encoding a protein that localises at the transition zone of primary cilia. Mutations in RPGRIP1L result in ciliopathies, severe human diseases caused by dysfunctional cilia. Patients with mutations in this gene often suffer from an impaired development of not only one but various organs. To elucidate the function of Rpgrip1l in human development and the mechanisms...

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Identifiers

PMID: 30075108
DOI: 10.1016/j.ydbio.2018.07.024

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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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