A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channel

Title
A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channel
Authors
Keywords
-
Journal
HEART RHYTHM
Volume -, Issue -, Pages -
Publisher
Elsevier BV
Online
2018-08-30
DOI
10.1016/j.hrthm.2018.08.030

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