Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2005-11-7
pubmed:abstractText
The aim of the study was to assess underlying genetic cause(s), clinical features, and response to therapy in catecholaminergic polymorphic ventricular tachycardia (CPVT) probands.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1468-6244
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
42
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
863-70
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:16272262-Adolescent, pubmed-meshheading:16272262-Amino Acid Sequence, pubmed-meshheading:16272262-Bradycardia, pubmed-meshheading:16272262-Catecholamines, pubmed-meshheading:16272262-Child, pubmed-meshheading:16272262-Child, Preschool, pubmed-meshheading:16272262-Female, pubmed-meshheading:16272262-Humans, pubmed-meshheading:16272262-Male, pubmed-meshheading:16272262-Middle Aged, pubmed-meshheading:16272262-Molecular Sequence Data, pubmed-meshheading:16272262-Mutation, pubmed-meshheading:16272262-Polymorphism, Genetic, pubmed-meshheading:16272262-Ryanodine Receptor Calcium Release Channel, pubmed-meshheading:16272262-Sequence Homology, Amino Acid, pubmed-meshheading:16272262-Syncope, pubmed-meshheading:16272262-Tachycardia, pubmed-meshheading:16272262-Tachycardia, Ventricular
pubmed:year
2005
pubmed:articleTitle
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients.
pubmed:publicationType
Letter, Research Support, Non-U.S. Gov't