17876883

Source:http://linkedlifedata.com/resource/pubmed/id/17876883

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019202, umls-concept:C0020792, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0152035, umls-concept:C0205210, umls-concept:C0205314, umls-concept:C0679622, umls-concept:C1707520, umls-concept:C1707877
pubmed:issue	38
pubmed:dateCreated	2007-9-18
pubmed:abstractText	To study mutations in the P-type ATPase (ATP7B) gene responsible for Wilson disease (WD) in the Eastern Chinese population, and the possible correlation of specific mutations with clinical characteristics.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100883448
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphatases, http://linkedlifedata.com/resource/pubmed/chemical/Cation Transport Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Wilson disease protein
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	1007-9327
pubmed:author	pubmed-author:LiangGongG, pubmed-author:ShuiQuan-XiangQX, pubmed-author:YeShengS, pubmed-author:ZhouLin-FuLF
pubmed:issnType	Print
pubmed:day	14
pubmed:volume	13
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	5147-50
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:17876883-Adenosine Triphosphatases, pubmed-meshheading:17876883-Adolescent, pubmed-meshheading:17876883-Asian Continental Ancestry Group, pubmed-meshheading:17876883-Case-Control Studies, pubmed-meshheading:17876883-Cation Transport Proteins, pubmed-meshheading:17876883-Child, pubmed-meshheading:17876883-Child, Preschool, pubmed-meshheading:17876883-China, pubmed-meshheading:17876883-Female, pubmed-meshheading:17876883-Genetic Predisposition to Disease, pubmed-meshheading:17876883-Genetic Testing, pubmed-meshheading:17876883-Genotype, pubmed-meshheading:17876883-Hepatolenticular Degeneration, pubmed-meshheading:17876883-Humans, pubmed-meshheading:17876883-Liver, pubmed-meshheading:17876883-Male, pubmed-meshheading:17876883-Mutation, pubmed-meshheading:17876883-Phenotype, pubmed-meshheading:17876883-Sequence Analysis, DNA
pubmed:year	2007
pubmed:articleTitle	Wilson disease: identification of two novel mutations and clinical correlation in Eastern Chinese patients.
pubmed:affiliation	Department of Pediatrics, Child Hospital, Zhejiang University, Hangzhou 310005, Zhejiang Province, China.
pubmed:publicationType	Journal Article