Linked Life Data

16029385

Source:http://linkedlifedata.com/resource/pubmed/id/16029385

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2005-7-20
pubmed:abstractText
To describe the clinical, genetic, and electrophysiologic characteristics of a new PAS-domain HERG mutation (M124R) that has been identified in a single large Jewish family with Long QT syndrome (LQTS).
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1082-720X
pubmed:author
pubmed:issnType
Print
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
334-41
pubmed:dateRevised
2010-12-3
pubmed:meshHeading
pubmed-meshheading:16029385-Adolescent, pubmed-meshheading:16029385-Adult, pubmed-meshheading:16029385-Aged, pubmed-meshheading:16029385-Aged, 80 and over, pubmed-meshheading:16029385-Child, pubmed-meshheading:16029385-Child, Preschool, pubmed-meshheading:16029385-Electrocardiography, pubmed-meshheading:16029385-Ether-A-Go-Go Potassium Channels, pubmed-meshheading:16029385-Female, pubmed-meshheading:16029385-Genotype, pubmed-meshheading:16029385-Humans, pubmed-meshheading:16029385-Infant, pubmed-meshheading:16029385-Israel, pubmed-meshheading:16029385-Long QT Syndrome, pubmed-meshheading:16029385-Male, pubmed-meshheading:16029385-Middle Aged, pubmed-meshheading:16029385-Mutation, pubmed-meshheading:16029385-Pedigree, pubmed-meshheading:16029385-Phenotype, pubmed-meshheading:16029385-Potassium Channels, Voltage-Gated, pubmed-meshheading:16029385-Sequence Analysis
pubmed:year
2005
pubmed:articleTitle
Clinical, genetic, and electrophysiologic characteristics of a new PAS-domain HERG mutation (M124R) causing Long QT syndrome.
pubmed:affiliation
Department of Genetics, The Life Sciences Institute, The Hebrew University, Jerusalem, Israel.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, N.I.H., Extramural