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Article

Function of Rieger syndrome gene in left-right asymmetry and craniofacial development.

Nature - 16 Sept 1999

Lu M F, Pressman C, Dyer R, Johnson R L, Martin J F

Abstract excerpt

Rieger syndrome, an autosomal dominant disorder, includes ocular, craniofacial and umbilical abnormalities. The pitx2 homeobox gene, which is mutated in Rieger syndrome, has been proposed to be the effector molecule interpreting left-right axial information from the early embryonic trunk to each...

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Source

Identifiers

PMID: 10499585
DOI: 10.1038/45797

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-10499585-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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