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

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

Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: HeartRhythm Case Reports - Volume 2, Issue 2, March 2016, Pages 128-131

Kiona Y. MD, Victoria L. MD, MPH, Maully J. MBBS, Matthew J. MD,