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Article

Screening for mutations of Axenfeld-Rieger syndrome caused by FOXC1 gene in Japanese patients.

Journal of glaucoma - 1 Dec 2001

Kawase C, Kawase K, Taniguchi T, Sugiyama K, Yamamoto T, Kitazawa Y, Alward W L, Stone E M, Nishimura D Y, Sheffield V C

Abstract excerpt

PURPOSE: Mutations in the forkhead transcription factor gene (FOXC1) have been recently shown to cause some cases of juvenile glaucoma associated with a variety of anterior-segment anomalies. The purpose of this study was to investigate the clinical features of Axenfeld-Rieger syndrome caused by FOXC1 mutations in Japanese patients. PATIENTS AND METHODS: After informed consent was obtained, genomic DNA was...

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Source

Identifiers

PMID: 11740218
DOI: 10.1097/00061198-200112000-00007

Genes

FOXC1

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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