Literature DB >> 10471492

Cardiac conduction defects associate with mutations in SCN5A.

J J Schott1, C Alshinawi, F Kyndt, V Probst, T M Hoorntje, M Hulsbeek, A A Wilde, D Escande, M M Mannens, H Le Marec.   

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Year:  1999        PMID： 10471492     DOI： 10.1038/12618

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  127 in total

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Review 10.  Brugada and long QT-3 syndromes: two phenotypes of the sodium channel disease.

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