reference/8669057

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8669057

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publicationName	Molecular vision
startingPage	1320
bibliographicCitation	Yang G, Zhang G, Wu Q, Zhao J. A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family. Mol Vis. 2011;17():1320–3. PMID: 21647270; PMCID: PMC3107997.
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date	2011
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC3107997 https://pubmed.ncbi.nlm.nih.gov/21647270
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/
title	A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family
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Total number of triples: 49.