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Article

SCN5A R1193Q polymorphism associated with progressive cardiac conduction defects and long QT syndrome in a Chinese family.

Journal of medical genetics - 1 Feb 2008

Sun A, Xu L, Wang S, Wang K, Huang W, Wang Y, Zou Y, Ge J

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Share to Arrhythmias, Cardiac
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 18245395
DOI: 10.1136/jmg.2007.056333

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SCN5A R1193Q polymorphism associated with progressive cardiac conduction defects and long QT syndrome in a Chinese family.PMID 18245395Read ↗

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[A case of long QT syndrome with atypical clinical phenotype caused by KCNQ1-R555C missense mutation].Semantic proximity Read ↗

Polymorphism H558R in the human cardiac sodium channel SCN5A gene is associated with atrial fibrillation.Semantic proximity Read ↗

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