reference/24215467

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publicationName	Molecular vision
startingPage	2570
bibliographicCitation	Khan AO, Aldahmesh MA, Alkuraya FS. Congenital megalocornea with zonular weakness and childhood lens-related secondary glaucoma - a distinct phenotype caused by recessive LTBP2 mutations. Mol Vis. 2011;17():2570–9. PMID: 22025892; PMCID: PMC3198484.
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date	2011
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/
title	Congenital megalocornea with zonular weakness and childhood lens-related secondary glaucoma - a distinct phenotype caused by recessive LTBP2 mutations
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