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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
11
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pubmed:dateCreated |
2005-10-21
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pubmed:abstractText |
Brugada syndrome (BS) is an electrical cardiac disorder with a right bundle branch block and ST segment elevation in leads V1 to V3 on surface electrocardiograms (ECGs), and is a syndrome that may lead to sudden cardiac death.
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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 |
Sep
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pubmed:issn |
0828-282X
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pubmed:author |
pubmed-author:BarraneFatima-ZaharaFZ,
pubmed-author:BrinkMarijkeM,
pubmed-author:ChahineMohamedM,
pubmed-author:GouasLaetitiaL,
pubmed-author:GuicheneyPascaleP,
pubmed-author:KellerDagmar IDI,
pubmed-author:MartinJohannieJ,
pubmed-author:OsswaldStefanS,
pubmed-author:PiloteSylvieS,
pubmed-author:SchwickNicolaN,
pubmed-author:SuarezVivianV
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pubmed:issnType |
Print
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pubmed:volume |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
925-31
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pubmed:dateRevised |
2011-7-22
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pubmed:meshHeading |
pubmed-meshheading:16239976-Adolescent,
pubmed-meshheading:16239976-Adult,
pubmed-meshheading:16239976-Ajmaline,
pubmed-meshheading:16239976-Anti-Arrhythmia Agents,
pubmed-meshheading:16239976-Bundle-Branch Block,
pubmed-meshheading:16239976-Cell Line,
pubmed-meshheading:16239976-Codon, Nonsense,
pubmed-meshheading:16239976-Death, Sudden, Cardiac,
pubmed-meshheading:16239976-Electrocardiography,
pubmed-meshheading:16239976-Female,
pubmed-meshheading:16239976-Heart Diseases,
pubmed-meshheading:16239976-Humans,
pubmed-meshheading:16239976-Male,
pubmed-meshheading:16239976-Microscopy, Fluorescence,
pubmed-meshheading:16239976-Middle Aged,
pubmed-meshheading:16239976-Molecular Biology,
pubmed-meshheading:16239976-Muscle Proteins,
pubmed-meshheading:16239976-Mutagenesis,
pubmed-meshheading:16239976-Patch-Clamp Techniques,
pubmed-meshheading:16239976-Pedigree,
pubmed-meshheading:16239976-Phenotype,
pubmed-meshheading:16239976-Sodium Channels,
pubmed-meshheading:16239976-Syndrome,
pubmed-meshheading:16239976-Transfection
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pubmed:year |
2005
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pubmed:articleTitle |
A novel nonsense mutation in the SCN5A gene leads to Brugada syndrome and a silent gene mutation carrier state.
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pubmed:affiliation |
Institut national de la santé et de la recherche médicale U582, Institut Fédératif de Recherche No 14, Pitié-Salpêtrière Hospital, Paris, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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