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
|