Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect
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| Description | scientific article published on 05 July 2016 |
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author: Martin Borggrefe Christian Wolpert Rainer Schimpf Elena Burashnikov Christian Veltmann Charles Antzelevitch |
| Publication date | July 5, 2016 |
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