21174522

Source:http://linkedlifedata.com/resource/pubmed/id/21174522

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0152035, umls-concept:C0392557, umls-concept:C0439660, umls-concept:C0796345, umls-concept:C1415075, umls-concept:C1513778
pubmed:issue	1
pubmed:dateCreated	2011-2-23
pubmed:abstractText	The aim of the study was to characterize the underlying mutation in a large multiplex Chinese family with hereditary nuclear cataract.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9436057
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Connexins, http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers, http://linkedlifedata.com/resource/pubmed/chemical/Eye Proteins, http://linkedlifedata.com/resource/pubmed/chemical/connexin 50
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1744-5094
pubmed:author	pubmed-author:BiY HYH, pubmed-author:ChenJiajingJ, pubmed-author:DaiQiushiQ, pubmed-author:HuSongnianS, pubmed-author:LingXuX, pubmed-author:Mse, pubmed-author:SeulBB, pubmed-author:WangDuen-MeiDM, pubmed-author:XuZ CZC, pubmed-author:ZhangFengF, pubmed-author:ZhuX NXN
pubmed:issnType	Electronic
pubmed:volume	32
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	48-53
pubmed:meshHeading	pubmed-meshheading:21174522-Adult, pubmed-meshheading:21174522-Asian Continental Ancestry Group, pubmed-meshheading:21174522-Base Sequence, pubmed-meshheading:21174522-Cataract, pubmed-meshheading:21174522-China, pubmed-meshheading:21174522-Chromosomes, Human, Pair 1, pubmed-meshheading:21174522-Connexins, pubmed-meshheading:21174522-DNA Mutational Analysis, pubmed-meshheading:21174522-DNA Primers, pubmed-meshheading:21174522-Eye Proteins, pubmed-meshheading:21174522-Female, pubmed-meshheading:21174522-Genetic Linkage, pubmed-meshheading:21174522-Genotype, pubmed-meshheading:21174522-Humans, pubmed-meshheading:21174522-Lens Nucleus, Crystalline, pubmed-meshheading:21174522-Lod Score, pubmed-meshheading:21174522-Male, pubmed-meshheading:21174522-Microsatellite Repeats, pubmed-meshheading:21174522-Molecular Sequence Data, pubmed-meshheading:21174522-Mutation, pubmed-meshheading:21174522-Pedigree
pubmed:year	2011
pubmed:articleTitle	Genetic linkage analyses and Cx50 mutation detection in a large multiplex Chinese family with hereditary nuclear cataract.
pubmed:affiliation	Shenyang He Eye Hospital, He College of Ophthalmology and Visual Science, Shenyang, China.
pubmed:publicationType	Journal Article