Brugada Syndrome and Calcium Channel Mutation in a Patient with Congenital Deaf Mutism
Date
2017Author
Canpolat, Uğur
Coteli, Cem
Aytemir, Kudret
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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.
URI
https://doi.org/10.1016/j.ipej.2017.01.002https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357834/
http://hdl.handle.net/11655/15480