Title : alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption.

Pub. Date : 2008 Aug

PMID : 19684871






1 Functional Relationships(s)
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1 METHODS AND RESULTS: Mutational analysis of SNTA1 was performed on 39 LQTS patients (QTc> or =480 ms) with previously negative genetic screening for the known LQTS-causing genes. qtc syntrophin alpha 1 Homo sapiens