15364333

Source:http://linkedlifedata.com/resource/pubmed/id/15364333

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015127, umls-concept:C0023976, umls-concept:C1314792, umls-concept:C1881250
pubmed:issue	6
pubmed:dateCreated	2004-9-14
pubmed:abstractText	The purpose of this research was to determine whether an intronic variant (T1945+6C) in KCNH2 is a disease-causing mutation, and if expanded phenotyping criteria produce improved identification of long QT syndrome (LQTS) patients.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/HL52338, http://linkedlifedata.com/resource/pubmed/grant/R01 HL46401, http://linkedlifedata.com/resource/pubmed/grant/R01 HL60723
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8301365
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/ERG1 potassium channel, http://linkedlifedata.com/resource/pubmed/chemical/Ether-A-Go-Go Potassium Channels, http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels, http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels, Voltage-Gated, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Complementary, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	0735-1097
pubmed:author	pubmed-author:AnsonBlake DBD, pubmed-author:BaralleFrancisco EFE, pubmed-author:BaralleMarcoM, pubmed-author:BensonD WoodrowDW, pubmed-author:CarlquistJohnJ, pubmed-author:JanuaryCraig TCT, pubmed-author:KeatingMark TMT, pubmed-author:SplawskiIgorI, pubmed-author:TimothyKatherine WKW, pubmed-author:VincentG MichaelGM, pubmed-author:WhitingBryantB, pubmed-author:ZhangLiL
pubmed:issnType	Print
pubmed:day	15
pubmed:volume	44
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1283-91
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:15364333-Adult, pubmed-meshheading:15364333-Aged, pubmed-meshheading:15364333-Aged, 80 and over, pubmed-meshheading:15364333-DNA Mutational Analysis, pubmed-meshheading:15364333-Electrocardiography, pubmed-meshheading:15364333-Ether-A-Go-Go Potassium Channels, pubmed-meshheading:15364333-Family Health, pubmed-meshheading:15364333-Follow-Up Studies, pubmed-meshheading:15364333-Genetic Linkage, pubmed-meshheading:15364333-Genetic Predisposition to Disease, pubmed-meshheading:15364333-Genotype, pubmed-meshheading:15364333-Heterozygote Detection, pubmed-meshheading:15364333-Humans, pubmed-meshheading:15364333-Introns, pubmed-meshheading:15364333-Long QT Syndrome, pubmed-meshheading:15364333-Male, pubmed-meshheading:15364333-Middle Aged, pubmed-meshheading:15364333-Mutation, pubmed-meshheading:15364333-Pedigree, pubmed-meshheading:15364333-Phenotype, pubmed-meshheading:15364333-Potassium Channels, pubmed-meshheading:15364333-Potassium Channels, Voltage-Gated, pubmed-meshheading:15364333-RNA, Complementary, pubmed-meshheading:15364333-RNA, Messenger, pubmed-meshheading:15364333-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:15364333-Statistics as Topic
pubmed:year	2004
pubmed:articleTitle	An intronic mutation causes long QT syndrome.
pubmed:affiliation	LDS Hospital, Salt Lake City, Utah 84103, USA.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't, Evaluation Studies