18713323

Source:http://linkedlifedata.com/resource/pubmed/id/18713323

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0035828, umls-concept:C0043157, umls-concept:C1556094, umls-concept:C1708943, umls-concept:C1853719, umls-concept:C2697834
pubmed:issue	3
pubmed:dateCreated	2008-8-20
pubmed:abstractText	Ethnic differences may affect the phenotypic expression of genetic disorders. However, data regarding the effect of ethnicity on outcome in patients with genetic cardiac disorders are limited. We compared the clinical course of Caucasian and Japanese long QT type-1 (LQT1) patients who were matched for mutations in the KCNQ1 gene.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/HL-33843, http://linkedlifedata.com/resource/pubmed/grant/HL-51618, http://linkedlifedata.com/resource/pubmed/grant/R01 HL033843-20A1
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pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9607443
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/KCNQ1 Potassium Channel
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1542-474X
pubmed:author	pubmed-author:AndrewsMark LML, pubmed-author:GoldenbergIlanI, pubmed-author:HofmanNynkeN, pubmed-author:LiuJudy FJF, pubmed-author:McNittScottS, pubmed-author:MiyamatoYoshihiroY, pubmed-author:MossArthur JAJ, pubmed-author:RobinsonJennifer LJL, pubmed-author:ShimizuWataruW, pubmed-author:WildeArthur AAA, pubmed-author:ZarebaWojciechW
pubmed:issnType	Electronic
pubmed:volume	13
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	234-41
pubmed:dateRevised	2011-9-26
pubmed:meshHeading	pubmed-meshheading:18713323-Asian Continental Ancestry Group, pubmed-meshheading:18713323-Chi-Square Distribution, pubmed-meshheading:18713323-Cohort Studies, pubmed-meshheading:18713323-Electrocardiography, pubmed-meshheading:18713323-European Continental Ancestry Group, pubmed-meshheading:18713323-Female, pubmed-meshheading:18713323-Genetic Predisposition to Disease, pubmed-meshheading:18713323-Genetic Variation, pubmed-meshheading:18713323-Humans, pubmed-meshheading:18713323-Incidence, pubmed-meshheading:18713323-KCNQ1 Potassium Channel, pubmed-meshheading:18713323-Kaplan-Meier Estimate, pubmed-meshheading:18713323-Long QT Syndrome, pubmed-meshheading:18713323-Male, pubmed-meshheading:18713323-Multivariate Analysis, pubmed-meshheading:18713323-Phenotype, pubmed-meshheading:18713323-Point Mutation, pubmed-meshheading:18713323-Polymorphism, Single Nucleotide, pubmed-meshheading:18713323-Prognosis, pubmed-meshheading:18713323-Proportional Hazards Models, pubmed-meshheading:18713323-Registries, pubmed-meshheading:18713323-Risk Assessment, pubmed-meshheading:18713323-Survival Analysis
pubmed:year	2008
pubmed:articleTitle	Phenotypic variability in Caucasian and Japanese patients with matched LQT1 mutations.
pubmed:affiliation	Cardiology Division of the Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY14642, USA.
pubmed:publicationType	Journal Article, Comparative Study, Research Support, N.I.H., Extramural