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Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism.
Indian Pacing and Electrophysiology Journal 2017 January
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 (Cav 1.2α1)] was identified.
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