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Whole-exome Sequencing and Electrophysiological Study Reveal a Novel Loss-of-function Mutation of KCNA10 in Epinephrine Provoked Long QT Syndrome with Familial History of Sudden Cardiac Death.

LEGAL MEDICINE(2023)

Cited 1|Views40
Key words
Long QT syndrome,KCNA10,K V 1,Mutation,Electrophysiology,Sudden cardiac death
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