17587269

Source:http://linkedlifedata.com/resource/pubmed/id/17587269

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008115, umls-concept:C0017920, umls-concept:C0021289, umls-concept:C0796357
pubmed:issue	4
pubmed:dateCreated	2007-6-25
pubmed:abstractText	Glucose-6-phosphate dehydrogenase (G6PD) deficiency, one of the most common human enzymatic defects, is characterized by extreme molecular and biochemical heterogeneity. The underlying DNA changes associated with G6PD deficiency in Asian subjects have not been extensively investigated.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100886002
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	1328-8067
pubmed:author	pubmed-author:DengBingB, pubmed-author:GuoChun-BaoCB, pubmed-author:LauY KYK, pubmed-author:XuYou-HuaYH, pubmed-author:YuJia-LinJL
pubmed:issnType	Print
pubmed:volume	49
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	463-7
pubmed:dateRevised	2008-5-21
pubmed:meshHeading	pubmed-meshheading:17587269-Asian Continental Ancestry Group, pubmed-meshheading:17587269-China, pubmed-meshheading:17587269-Female, pubmed-meshheading:17587269-Glucosephosphate Dehydrogenase Deficiency, pubmed-meshheading:17587269-Humans, pubmed-meshheading:17587269-Infant, Newborn, pubmed-meshheading:17587269-Male, pubmed-meshheading:17587269-Mutation
pubmed:year	2007
pubmed:articleTitle	Three mutations analysis of glucose-6-phosphate dehydrogenase deficiency in neonates in South-west China.
pubmed:affiliation	Department of Neonate, Children's Hospital, Chongqing Medical University, Chongqing, China.
pubmed:publicationType	Journal Article