reference/19434990

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publicationName	Molecular vision
startingPage	549
bibliographicCitation	Anjum I, Eiberg H, Baig SM, Tommerup N, Hansen L. A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family. Mol Vis. 2010 Mar 30;16():549–55. PMID: 20361012; PMCID: PMC2846847.
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date	2010-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC2846847 https://pubmed.ncbi.nlm.nih.gov/20361012
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/
title	A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family
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