Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism.

To the best of our knowledge, for the first time in the literature, we described a congenitally deaf-mute patient with Brugada syndrome (BrS) in whom a mutation in L-type Ca+2 channel [CACNA1C (Cav1.2α1)] was identified. Copyright © 2017 Indian Heart Rhythm Society. Production and hosting by Elsevier B.V. All rights reserved.

Citation

Uğur Canpolat, Cem Coteli, Kudret Aytemir. Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism. Indian pacing and electrophysiology journal. 2017 Jan 01;17(1):16-17

PMID: 28401855

search → result