|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
3
|
|
pubmed:dateCreated |
2007-3-7
|
|
pubmed:abstractText |
Long QT syndromes (LQTS) are inherited diseases involving mutations to genes encoding a number of cardiac ion channels and a membrane adaptor protein. The MinK protein is a cardiac K-channel accessory subunit encoded by the KCNE1 gene, mutations of which are associated with the LQT5 form of LQTS.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Mar
|
|
pubmed:issn |
1547-5271
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
4
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
332-40
|
|
pubmed:dateRevised |
2009-11-19
|
|
pubmed:meshHeading |
pubmed-meshheading:17341399-Adult,
pubmed-meshheading:17341399-Aged,
pubmed-meshheading:17341399-Asian Continental Ancestry Group,
pubmed-meshheading:17341399-Chromatography, High Pressure Liquid,
pubmed-meshheading:17341399-Electrocardiography,
pubmed-meshheading:17341399-Electrophysiologic Techniques, Cardiac,
pubmed-meshheading:17341399-Ether-A-Go-Go Potassium Channels,
pubmed-meshheading:17341399-Female,
pubmed-meshheading:17341399-Gene Expression,
pubmed-meshheading:17341399-Genetic Testing,
pubmed-meshheading:17341399-Genotype,
pubmed-meshheading:17341399-Humans,
pubmed-meshheading:17341399-Japan,
pubmed-meshheading:17341399-KCNQ1 Potassium Channel,
pubmed-meshheading:17341399-Long QT Syndrome,
pubmed-meshheading:17341399-Mutation, Missense,
pubmed-meshheading:17341399-Phenotype,
pubmed-meshheading:17341399-Polymorphism, Single Nucleotide,
pubmed-meshheading:17341399-Potassium Channels, Voltage-Gated,
pubmed-meshheading:17341399-Research Design
|
|
pubmed:year |
2007
|
|
pubmed:articleTitle |
N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome.
|
|
pubmed:affiliation |
Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
|
|
pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|
