21823532

Source:http://linkedlifedata.com/resource/pubmed/id/21823532

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011155, umls-concept:C0020538, umls-concept:C0332282, umls-concept:C0522498
pubmed:issue	5-6
pubmed:dateCreated	2011-8-9
pubmed:abstractText	To investigate CYP 7A1 gene mutations in Chinese patients with 17alpha-hydroxylase deficiency.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9508900
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/CYP17A1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Steroid 17-alpha-Hydroxylase
pubmed:status	MEDLINE
pubmed:issn	0334-018X
pubmed:author	pubmed-author:FuJun-FenJF, pubmed-author:GongFang-QiFQ, pubmed-author:ShenZhengZ, pubmed-author:VighB JBJ, pubmed-author:ZhuWei-HuaWH
pubmed:issnType	Print
pubmed:volume	24
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	333-7
pubmed:meshHeading	pubmed-meshheading:21823532-Adolescent, pubmed-meshheading:21823532-Adrenal Hyperplasia, Congenital, pubmed-meshheading:21823532-Base Sequence, pubmed-meshheading:21823532-Child, pubmed-meshheading:21823532-Female, pubmed-meshheading:21823532-Genetic Association Studies, pubmed-meshheading:21823532-Humans, pubmed-meshheading:21823532-Hypertension, pubmed-meshheading:21823532-Male, pubmed-meshheading:21823532-Mutation, pubmed-meshheading:21823532-Mutation, Missense, pubmed-meshheading:21823532-Sequence Deletion, pubmed-meshheading:21823532-Sexual Infantilism, pubmed-meshheading:21823532-Steroid 17-alpha-Hydroxylase
pubmed:year	2011
pubmed:articleTitle	Rare hypertension as a result of 17alpha-hydroxylase deficiency.
pubmed:affiliation	Children's Hospital, Zhejiang University School of Medicine, Zhugan Xiang 57, Hangzhou 310003, P.R. China.
pubmed:publicationType	Journal Article, Review, Case Reports