Exome sequencing and systems biology converge to identify novel mutations in the L-type calcium channel, CACNA1C, linked to autosomal dominant long QT syndrome

Nicole J. Boczek, Jabe M. Best, David J. Tester, John R. Giudicessi, Sumit Middha, Jared M. Evans, Timothy J. Kamp, Michael J. Ackerman

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