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Brugada Syndrome and Calcium Channel Mutation in a Patient with Congenital Deaf Mutism
(2017)
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.