12812649

Source:http://linkedlifedata.com/resource/pubmed/id/12812649

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019202, umls-concept:C0030705, umls-concept:C0032659, umls-concept:C0152035, umls-concept:C2717879
pubmed:issue	4
pubmed:dateCreated	2003-6-18
pubmed:abstractText	To investigate the correlation between genotype and phenotype of patients with Wilson disease (WD) in the Chinese population.
pubmed:language	chi
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7511141
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	0376-2491
pubmed:author	pubmed-author:FangLingL, pubmed-author:LinMin-tingMT, pubmed-author:MurongShen-xingSX, pubmed-author:WangNingN, pubmed-author:WuZhi-yingZY
pubmed:issnType	Print
pubmed:day	25
pubmed:volume	83
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	309-11
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:12812649-Adolescent, pubmed-meshheading:12812649-Adult, pubmed-meshheading:12812649-Child, pubmed-meshheading:12812649-Child, Preschool, pubmed-meshheading:12812649-Female, pubmed-meshheading:12812649-Genotype, pubmed-meshheading:12812649-Hepatolenticular Degeneration, pubmed-meshheading:12812649-Humans, pubmed-meshheading:12812649-Male, pubmed-meshheading:12812649-Mutation, pubmed-meshheading:12812649-Phenotype, pubmed-meshheading:12812649-Polymerase Chain Reaction, pubmed-meshheading:12812649-Polymorphism, Single-Stranded Conformational
pubmed:year	2003
pubmed:articleTitle	[Genotype-phenotype correlation of patients with wilson disease in Chinese population].
pubmed:affiliation	Department of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou 350005 China.
pubmed:publicationType	Journal Article, English Abstract, Research Support, Non-U.S. Gov't