20019893

Source:http://linkedlifedata.com/resource/pubmed/id/20019893

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0009691, umls-concept:C0015576, umls-concept:C0026882, umls-concept:C0152035, umls-concept:C0205314, umls-concept:C0443147, umls-concept:C0678227, umls-concept:C0679622, umls-concept:C1415075
pubmed:dateCreated	2009-12-18
pubmed:abstractText	To identify the genetic defect associated with autosomal dominant congenital nuclear cataract in a Chinese family.
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pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9605351
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Connexins, http://linkedlifedata.com/resource/pubmed/chemical/Eye Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Mutant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/connexin 50
pubmed:status	MEDLINE
pubmed:issn	1090-0535
pubmed:author	pubmed-author:ChengJieJ, pubmed-author:HSUJ YJY, pubmed-author:SuoPeisuP, pubmed-author:WangBinbinB, pubmed-author:WangJingJ, pubmed-author:WangKaijieK, pubmed-author:ZhouShiyiS, pubmed-author:ZhuQiQ, pubmed-author:ZhuSiquanS
pubmed:issnType	Electronic
pubmed:volume	15
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2813-20
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:20019893-Humans, pubmed-meshheading:20019893-Adolescent, pubmed-meshheading:20019893-Cataract, pubmed-meshheading:20019893-Aged, pubmed-meshheading:20019893-Family, pubmed-meshheading:20019893-Child, pubmed-meshheading:20019893-Mutation, pubmed-meshheading:20019893-Child, Preschool, pubmed-meshheading:20019893-Asian Continental Ancestry Group, pubmed-meshheading:20019893-Female, pubmed-meshheading:20019893-China, pubmed-meshheading:20019893-Male, pubmed-meshheading:20019893-Adult, pubmed-meshheading:20019893-Middle Aged, pubmed-meshheading:20019893-Base Sequence, pubmed-meshheading:20019893-Young Adult, pubmed-meshheading:20019893-Eye Proteins, pubmed-meshheading:20019893-Pedigree, pubmed-meshheading:20019893-Amino Acid Sequence, pubmed-meshheading:20019893-Genes, Dominant