reference/15227929

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startingPage	43
bibliographicCitation	Komatireddy S, Chakrabarti S, Mandal AK, Reddy AB, Sampath S, Panicker SG, Balasubramanian D. Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India. Mol Vis. 2003 Feb 18;9():43–8. PMID: 12592227.
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date	2003-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/12592227
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/
title	Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India
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