Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report

https://doi.org/10.1016/j.hrcr.2015.10.011Get rights and content
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Keywords

Familial long QT syndrome
Dilated cardiomyopathy
KCNQ1
Voltage-gated potassium channel
Genetics

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