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Article

Axenfeld-Rieger Syndrome and Leukoencephalopathy Caused by a Mutation in FOXC1.

Pediatric neurology - 1 Jan 2017

Kumar Manish, Chambers Chelsea, Dhamija Radhika

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 27697311
DOI: 10.1016/j.pediatrneurol.2016.08.020

Genes

FOXC1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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