reference/30367582

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bibliographicCitation	Micheal S, Siddiqui SN, Zafar SN, Villanueva-Mendoza C, Cortés-González V, Khan MI, den Hollander AI. A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma. PLoS ONE. 2016 Jul 27;11(7):e0160016. doi: 10.1371/journal.pone.0160016.
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date	2016-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1371/journal.pone.0160016 https://pubmed.ncbi.nlm.nih.gov/27463523 https://pubmed.ncbi.nlm.nih.gov/PMC4963127
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
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