Mapping of a Gene for Long QT Syndrome to Chromosome 4q25-27

Long QT syndrome (LQTS) is a heterogeneous inherited disorder causing syncope and sudden death from ventricular arrhythmias. A first locus for this disorder was mapped to chromosome 11p15.5. However, locus heterogeneity has been demonstrated in several families, and two other loci have recently been...

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Detalhes bibliográficos
Main Authors: Schott, Jean-Jacques, Charpentier, Flavien, Peltier, Sophie, Foley, Patrick, Drouin, Emmanuel, Bouhour, Jean-Brieuc, Donnelly, Patricia, Vergnaud, Gilles, Bachner, Lucien, Moisan, Jean-Paul, Le Marec, Hervé, Pascal, Olivier
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801360/
https://ncbi.nlm.nih.gov/pubmed/7485162
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