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rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
2009-4-10
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pubmed:abstractText |
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe inherited cardiac disorder caused by mutations predominantly in the ryanodine receptor (RyR2) gene. We sought to identify mutations in genes affecting cardiac calcium cycling in patients with CPVT and in less typical familial exercise-related ventricular arrhythmias.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-10588221,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-11157710,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-11208676,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-12093772,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-12169647,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-12818578,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-12837242,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-14500331,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-14571276,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-15073377,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-15197150,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-15710754,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-15913575,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-15932750,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-16198846,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-16239587,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-16314582,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-16314583,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-17875969,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19216760-17956252
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1471-2350
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
12
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:19216760-Adolescent,
pubmed-meshheading:19216760-Adult,
pubmed-meshheading:19216760-Catecholamines,
pubmed-meshheading:19216760-Child,
pubmed-meshheading:19216760-Child, Preschool,
pubmed-meshheading:19216760-Electrocardiography,
pubmed-meshheading:19216760-Exons,
pubmed-meshheading:19216760-Female,
pubmed-meshheading:19216760-Humans,
pubmed-meshheading:19216760-Male,
pubmed-meshheading:19216760-Middle Aged,
pubmed-meshheading:19216760-Mutation, Missense,
pubmed-meshheading:19216760-Phenotype,
pubmed-meshheading:19216760-Ryanodine Receptor Calcium Release Channel,
pubmed-meshheading:19216760-Tachycardia, Ventricular,
pubmed-meshheading:19216760-Ventricular Premature Complexes,
pubmed-meshheading:19216760-Young Adult
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pubmed:year |
2009
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pubmed:articleTitle |
Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia.
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pubmed:affiliation |
Department of Cardiology, University of Helsinki, Helsinki, Finland. annukka.marjamaa@helsinki.fi
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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