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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2006-1-9
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pubmed:abstractText |
The numerous mutations in the long QT syndrome (LQTS)-associated genes reported to date are point mutations or small insertions and deletions in coding regions or at splice junctions.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1547-5271
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
52-5
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pubmed:dateRevised |
2009-10-27
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pubmed:meshHeading |
pubmed-meshheading:16399053-Adolescent,
pubmed-meshheading:16399053-Adult,
pubmed-meshheading:16399053-DNA Mutational Analysis,
pubmed-meshheading:16399053-Ether-A-Go-Go Potassium Channels,
pubmed-meshheading:16399053-Exons,
pubmed-meshheading:16399053-Female,
pubmed-meshheading:16399053-Gene Duplication,
pubmed-meshheading:16399053-Gene Rearrangement,
pubmed-meshheading:16399053-Humans,
pubmed-meshheading:16399053-KCNQ1 Potassium Channel,
pubmed-meshheading:16399053-Long QT Syndrome,
pubmed-meshheading:16399053-Netherlands,
pubmed-meshheading:16399053-Nucleic Acid Amplification Techniques
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pubmed:year |
2006
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pubmed:articleTitle |
Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies.
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pubmed:affiliation |
Experimental and Molecular Cardiology Group, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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