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Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism
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(v)1.2α1)] was identified.
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| Pubblicato in: | Indian Pacing Electrophysiol J |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5357834/ https://ncbi.nlm.nih.gov/pubmed/28401855 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ipej.2017.01.002 |
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