21811973

Source:http://linkedlifedata.com/resource/pubmed/id/21811973

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0030705, umls-concept:C0268595, umls-concept:C0796357, umls-concept:C1415009
pubmed:issue	4
pubmed:dateCreated	2011-8-3
pubmed:abstractText	To investigate the mutations of glutaryl-CoA dehydrogenase (GCDH) gene in patients with glutaric aciduria type I(GA-1).
pubmed:language	chi
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9425197
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Glutaryl-CoA Dehydrogenase
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	1003-9406
pubmed:author	pubmed-author:ChenJingJ, pubmed-author:HuangYi-ningYN, pubmed-author:WangZhao-xiaZX, pubmed-author:YangYan-lingYL, pubmed-author:ZhangJin-liJL
pubmed:issnType	Print
pubmed:volume	28
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	374-8
pubmed:meshHeading	pubmed-meshheading:21811973-Adult, pubmed-meshheading:21811973-Amino Acid Metabolism, Inborn Errors, pubmed-meshheading:21811973-Amino Acid Sequence, pubmed-meshheading:21811973-Animals, pubmed-meshheading:21811973-Base Sequence, pubmed-meshheading:21811973-Brain Diseases, Metabolic, pubmed-meshheading:21811973-DNA Mutational Analysis, pubmed-meshheading:21811973-Exons, pubmed-meshheading:21811973-Female, pubmed-meshheading:21811973-Glutaryl-CoA Dehydrogenase, pubmed-meshheading:21811973-Humans, pubmed-meshheading:21811973-Infant, pubmed-meshheading:21811973-Male, pubmed-meshheading:21811973-Molecular Sequence Data
pubmed:year	2011
pubmed:articleTitle	[Mutation analysis of GCDH gene in eight patients with glutaric aciduria type I].
pubmed:affiliation	Department of Neurology, First Hospital, Peking University, Beijing 100034, P. R. China.
pubmed:publicationType	Journal Article, English Abstract, Case Reports