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

Kardiyoloji Anabilim Dalı

Araştırma sonucu: Dergiye katkı › Makale › bilirkişi

Özet

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.

Orijinal dil	İngilizce
Sayfa (başlangıç-bitiş)	16-17
Sayfa sayısı	2
Dergi	Indian Pacing and Electrophysiology Journal
Hacim	17
Basın numarası	1
DOI'lar	https://doi.org/10.1016/j.ipej.2017.01.002
Yayın durumu	Yayınlandı - 1 Oca 2017

Belgeye Erişim

10.1016/j.ipej.2017.01.002

Diger dosyalar ve linkler

Link to publication in Scopus

Bundan alıntı yap

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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.",

keywords = "Brugada syndrome, Calcium channelopathy, Deaf and mute",

author = "Uğur Canpolat and Cem Coteli and Kudret Aytemir",

note = "Publisher Copyright: {\textcopyright} 2017 Indian Heart Rhythm Society",

year = "2017",

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doi = "10.1016/j.ipej.2017.01.002",

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AU - Canpolat, Uğur

AU - Coteli, Cem

AU - Aytemir, Kudret

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Y1 - 2017/1/1

N2 - 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.

AB - 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.

KW - Brugada syndrome

KW - Calcium channelopathy

KW - Deaf and mute

UR - https://www.scopus.com/pages/publications/85009753169

U2 - 10.1016/j.ipej.2017.01.002

DO - 10.1016/j.ipej.2017.01.002

M3 - Article

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JO - Indian Pacing and Electrophysiology Journal

JF - Indian Pacing and Electrophysiology Journal

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

Özet

Belgeye Erişim

Diger dosyalar ve linkler

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