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HeartRhythm Case Reports
(Mar 2016)
Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report
Kiona Y. Allen, MD,
Victoria L. Vetter, MD, MPH,
Maully J. Shah, MBBS,
Matthew J. O’Connor, MD
Affiliations
Kiona Y. Allen, MD
Victoria L. Vetter, MD, MPH
Maully J. Shah, MBBS
Matthew J. O’Connor, MD
DOI
https://doi.org/10.1016/j.hrcr.2015.10.011
Journal volume & issue
Vol. 2, no. 2
pp. 128 – 131
Abstract
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No abstracts available.
Keywords
Familial long QT syndrome
Dilated cardiomyopathy
KCNQ1
Voltage-gated potassium channel
Genetics
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