11739969

Source:http://linkedlifedata.com/resource/pubmed/id/11739969

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015528, umls-concept:C0035302, umls-concept:C0035820, umls-concept:C1882417
pubmed:issue	12
pubmed:dateCreated	2001-12-13
pubmed:abstractText	Factor XIII (FXIII) Val34Leu, a common polymorphism in the gene for factor XIII, has been associated with a lower risk of stroke, myocardial infarction, and deep vein thrombosis. Ineffective fibrin cross-linking has been suggested to be causative. The aim of the present case-control study was to investigate the role of FXIII Val34Leu polymorphism in patients with retinal artery occlusion.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0235266
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Factor XIII
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	1524-4628
pubmed:author	pubmed-author:DeutschmannHH, pubmed-author:HaasAA, pubmed-author:RennerWW, pubmed-author:SchmutOO, pubmed-author:StangelII, pubmed-author:WascherT CTC, pubmed-author:WegerMM
pubmed:issnType	Electronic
pubmed:day	1
pubmed:volume	32
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2759-61
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:11739969-Adult, pubmed-meshheading:11739969-Age Distribution, pubmed-meshheading:11739969-Aged, pubmed-meshheading:11739969-Aged, 80 and over, pubmed-meshheading:11739969-Alleles, pubmed-meshheading:11739969-Amino Acid Substitution, pubmed-meshheading:11739969-Case-Control Studies, pubmed-meshheading:11739969-Factor XIII, pubmed-meshheading:11739969-Female, pubmed-meshheading:11739969-Gene Frequency, pubmed-meshheading:11739969-Genetic Testing, pubmed-meshheading:11739969-Genotype, pubmed-meshheading:11739969-Homozygote, pubmed-meshheading:11739969-Humans, pubmed-meshheading:11739969-Immunity, Innate, pubmed-meshheading:11739969-Male, pubmed-meshheading:11739969-Middle Aged, pubmed-meshheading:11739969-Odds Ratio, pubmed-meshheading:11739969-Polymerase Chain Reaction, pubmed-meshheading:11739969-Polymorphism, Genetic, pubmed-meshheading:11739969-Prevalence, pubmed-meshheading:11739969-Retinal Artery Occlusion, pubmed-meshheading:11739969-Retrospective Studies, pubmed-meshheading:11739969-Risk Factors, pubmed-meshheading:11739969-Sex Distribution
pubmed:year	2001
pubmed:articleTitle	Role of factor XIII Val34Leu polymorphism in retinal artery occlusion.
pubmed:affiliation	Department of Ophthalmology, Auenbruggerplatz 4, A-80365 Graz, Austria. martin.weger@kfunigraz.ac.at
pubmed:publicationType	Journal Article