17991432

Source:http://linkedlifedata.com/resource/pubmed/id/17991432

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011155, umls-concept:C0026882, umls-concept:C0205082, umls-concept:C1412468, umls-concept:C1867743
pubmed:issue	1-2
pubmed:dateCreated	2007-12-24
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/1302422
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/APOA1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Apolipoprotein A-I
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	0009-8981
pubmed:author	pubmed-author:AlallónWalterW, pubmed-author:EsperónPatriciaP, pubmed-author:RaggioVíctorV, pubmed-author:StollMarioM, pubmed-author:VitalMarceloM
pubmed:issnType	Print
pubmed:volume	388
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	222-4
pubmed:meshHeading	pubmed-meshheading:17991432-Adult, pubmed-meshheading:17991432-Aged, pubmed-meshheading:17991432-Aged, 80 and over, pubmed-meshheading:17991432-Apolipoprotein A-I, pubmed-meshheading:17991432-Coronary Artery Disease, pubmed-meshheading:17991432-Female, pubmed-meshheading:17991432-Humans, pubmed-meshheading:17991432-Hypoalphalipoproteinemias, pubmed-meshheading:17991432-Male, pubmed-meshheading:17991432-Middle Aged, pubmed-meshheading:17991432-Mutation, pubmed-meshheading:17991432-Pedigree
pubmed:year	2008
pubmed:articleTitle	A new APOA1 mutation with severe HDL-cholesterol deficiency and premature coronary artery disease.
pubmed:publicationType	Letter