|
rdf:type |
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lifeskim:mentions |
umls-concept:C0006675,
umls-concept:C0011900,
umls-concept:C0017431,
umls-concept:C0023976,
umls-concept:C0030685,
umls-concept:C0030705,
umls-concept:C0054493,
umls-concept:C0079941,
umls-concept:C0205160,
umls-concept:C0391871,
umls-concept:C0439799,
umls-concept:C0680255,
umls-concept:C0936012,
umls-concept:C1283071,
umls-concept:C1631597,
umls-concept:C1880156,
umls-concept:C1963578
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pubmed:issue |
22
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pubmed:dateCreated |
2009-11-20
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pubmed:abstractText |
This study was undertaken to determine the spectrum and prevalence of mutations in the RYR2-encoded cardiac ryanodine receptor in cases with exertional syncope and normal corrected QT interval (QTc).
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
|
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pubmed:issn |
1558-3597
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pubmed:author |
|
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pubmed:issnType |
Electronic
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pubmed:day |
24
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pubmed:volume |
54
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2065-74
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pubmed:dateRevised |
2011-3-3
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pubmed:meshHeading |
pubmed-meshheading:19926015-Adult,
pubmed-meshheading:19926015-Calcium Channels,
pubmed-meshheading:19926015-Catecholamines,
pubmed-meshheading:19926015-DNA Mutational Analysis,
pubmed-meshheading:19926015-Death, Sudden, Cardiac,
pubmed-meshheading:19926015-Exercise,
pubmed-meshheading:19926015-Exercise Test,
pubmed-meshheading:19926015-Female,
pubmed-meshheading:19926015-Genetic Predisposition to Disease,
pubmed-meshheading:19926015-Genotype,
pubmed-meshheading:19926015-Humans,
pubmed-meshheading:19926015-Long QT Syndrome,
pubmed-meshheading:19926015-Male,
pubmed-meshheading:19926015-Mosaicism,
pubmed-meshheading:19926015-Open Reading Frames,
pubmed-meshheading:19926015-Ryanodine Receptor Calcium Release Channel,
pubmed-meshheading:19926015-Syncope,
pubmed-meshheading:19926015-Tachycardia, Ventricular,
pubmed-meshheading:19926015-Young Adult
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pubmed:year |
2009
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pubmed:articleTitle |
The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysis.
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pubmed:affiliation |
Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota 55905, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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