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Circ Cardiovasc Genet. 2013 Jun;6(3):227-9. doi: 10.1161/CIRCGENETICS.113.000199.

Taming rare variation with known biology in long QT syndrome.

Perez MV, Ashley EA.

KEYWORDS:

Editorials; bioinformatics; genetics; long QT syndrome

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Exome sequencing and systems biology converge to identify novel mutations in the L-type calcium channel, CACNA1C, linked to autosomal dominant long QT syndrome. [Circ Cardiovasc Genet. 2013]

PMID:: 23778589
DOI:: 10.1161/CIRCGENETICS.113.000199

[Indexed for MEDLINE]

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Long QT Syndrome - Genetic Alliance

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