Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2006-10-25
pubmed:abstractText
Mutations of the cardiac ryanodine receptor type 2 (RyR2) gene are known to cause effort-induced polymorphic ventricular arrhythmia, syncope and sudden death.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1346-9843
pubmed:author
pubmed:issnType
Print
pubmed:volume
70
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1402-6
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:17062961-Adolescent, pubmed-meshheading:17062961-Adult, pubmed-meshheading:17062961-Autopsy, pubmed-meshheading:17062961-Cardiovascular System, pubmed-meshheading:17062961-Cause of Death, pubmed-meshheading:17062961-Child, pubmed-meshheading:17062961-Child, Preschool, pubmed-meshheading:17062961-DNA Mutational Analysis, pubmed-meshheading:17062961-Death, Sudden, Cardiac, pubmed-meshheading:17062961-Diagnosis, pubmed-meshheading:17062961-Exons, pubmed-meshheading:17062961-Female, pubmed-meshheading:17062961-Genetic Testing, pubmed-meshheading:17062961-Humans, pubmed-meshheading:17062961-Lymphatic System, pubmed-meshheading:17062961-Male, pubmed-meshheading:17062961-Mutation, Missense, pubmed-meshheading:17062961-Ryanodine Receptor Calcium Release Channel, pubmed-meshheading:17062961-Thymus Gland
pubmed:year
2006
pubmed:articleTitle
Postmortem molecular screening for cardiac ryanodine receptor type 2 mutations in sudden unexplained death: R420W mutated case with characteristics of status thymico-lymphatics.
pubmed:affiliation
Department of Legal Medicine, Osaka Medical College, Takatsuki 569-8686, Japan. leg010@art.osaka-med.ac.jp
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't