| dc.contributor.author | Canpolat, Uğur | |
| dc.contributor.author | Coteli, Cem | |
| dc.contributor.author | Aytemir, Kudret | |
| dc.date.accessioned | 2019-12-10T11:21:29Z | |
| dc.date.available | 2019-12-10T11:21:29Z | |
| dc.date.issued | 2017 | |
| dc.identifier.issn | 0972-6292 | |
| dc.identifier.uri | https://doi.org/10.1016/j.ipej.2017.01.002 | |
| dc.identifier.uri | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357834/ | |
| dc.identifier.uri | http://hdl.handle.net/11655/15480 | |
| dc.description.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. | |
| dc.relation.isversionof | 10.1016/j.ipej.2017.01.002 | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.title | Brugada Syndrome and Calcium Channel Mutation in a Patient with Congenital Deaf Mutism | |
| dc.type | info:eu-repo/semantics/article | |
| dc.type | info:eu-repo/semantics/publishedVersion | |
| dc.relation.journal | Indian Pacing and Electrophysiology Journal | |
| dc.contributor.department | Kardiyoloji | |
| dc.identifier.volume | 17 | |
| dc.identifier.issue | 1 | |
| dc.identifier.startpage | 16 | |
| dc.identifier.endpage | 17 | |
| dc.description.index | PubMed | |
| dc.description.index | Scopus | |
