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

Uğur Canpolat; Cem Coteli; Kudret Aytemir

doi:10.1016/j.ipej.2017.01.002

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

Division of Cardiology

Research output: Contribution to journal › Article › peer-review

Abstract

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 (Ca_v1.2α1)] was identified.

Original language	English
Pages (from-to)	16-17
Number of pages	2
Journal	Indian Pacing and Electrophysiology Journal
Volume	17
Issue number	1
DOIs	https://doi.org/10.1016/j.ipej.2017.01.002
Publication status	Published - 1 Jan 2017

Keywords

Brugada syndrome
Calcium channelopathy
Deaf and mute

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10.1016/j.ipej.2017.01.002

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title = "Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism",

abstract = "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.",

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AU - Coteli, Cem

AU - Aytemir, Kudret

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KW - Calcium channelopathy

KW - Deaf and mute

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

Abstract

Keywords

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