9067760

Source:http://linkedlifedata.com/resource/pubmed/id/9067760

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0030705, umls-concept:C0162735, umls-concept:C0205314, umls-concept:C0342464, umls-concept:C0678226, umls-concept:C0679622, umls-concept:C0852654, umls-concept:C1522419, umls-concept:C1706115, umls-concept:C1859991
pubmed:issue	2
pubmed:dateCreated	1997-5-21
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9215429
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/HLA Antigens, http://linkedlifedata.com/resource/pubmed/chemical/Steroid 21-Hydroxylase
pubmed:status	MEDLINE
pubmed:issn	1059-7794
pubmed:author	pubmed-author:DonohoueP APA, pubmed-author:Kirby-KeyserLL, pubmed-author:PorterC CCC
pubmed:issnType	Print
pubmed:volume	9
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	181-2
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:9067760-Adrenal Hyperplasia, Congenital, pubmed-meshheading:9067760-Blotting, Southern, pubmed-meshheading:9067760-Exons, pubmed-meshheading:9067760-HLA Antigens, pubmed-meshheading:9067760-Homozygote, pubmed-meshheading:9067760-Humans, pubmed-meshheading:9067760-Pedigree, pubmed-meshheading:9067760-Point Mutation, pubmed-meshheading:9067760-Polymerase Chain Reaction, pubmed-meshheading:9067760-Restriction Mapping, pubmed-meshheading:9067760-Sequence Analysis, DNA, pubmed-meshheading:9067760-Steroid 21-Hydroxylase
pubmed:year	1997
pubmed:articleTitle	E380D: a novel point mutation of CYP21 in an HLA-homozygous patient with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
pubmed:affiliation	Department of Pediatrics, University of Iowa College of Medicine, Iowa City 52242, USA.
pubmed:publicationType	Journal Article