Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2010-4-8
pubmed:abstractText
Sinus node dysfunction (SND) is a heterogeneous disorder of unknown etiology characterized by a variety of supraventricular arrhythmias with symptoms of syncope, palpitations, and dizziness. The mechanism underlying the abnormal rhythm is incompletely understood.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1421-9751
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
115
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
176-81
pubmed:meshHeading
pubmed-meshheading:20110696-Adolescent, pubmed-meshheading:20110696-Adult, pubmed-meshheading:20110696-Aged, pubmed-meshheading:20110696-Alleles, pubmed-meshheading:20110696-Amino Acid Substitution, pubmed-meshheading:20110696-DNA Mutational Analysis, pubmed-meshheading:20110696-Female, pubmed-meshheading:20110696-G Protein-Coupled Inwardly-Rectifying Potassium Channels, pubmed-meshheading:20110696-Genotype, pubmed-meshheading:20110696-Humans, pubmed-meshheading:20110696-Male, pubmed-meshheading:20110696-Middle Aged, pubmed-meshheading:20110696-Pacemaker, Artificial, pubmed-meshheading:20110696-Polymorphism, Genetic, pubmed-meshheading:20110696-Polymorphism, Single Nucleotide, pubmed-meshheading:20110696-Reference Values, pubmed-meshheading:20110696-Sequence Analysis, DNA, pubmed-meshheading:20110696-Sick Sinus Syndrome, pubmed-meshheading:20110696-Young Adult
pubmed:year
2010
pubmed:articleTitle
Genetic variation in the inwardly rectifying K channel subunits KCNJ3 (GIRK1) and KCNJ5 (GIRK4) in patients with sinus node dysfunction.
pubmed:affiliation
Laboratory of Molecular Cardiology, Copenhagen University Hospital, Copenhagen, Denmark.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't