E1784K mutation in SCN5A and overlap syndrome
- PMID: 24920323
- DOI: 10.1253/circj.cj-14-0564
E1784K mutation in SCN5A and overlap syndrome
Comment on
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High prevalence of the SCN5A E1784K mutation in school children with long QT syndrome living on the Okinawa islands.Circ J. 2014;78(8):1974-9. doi: 10.1253/circj.cj-13-1516. Epub 2014 May 28. Circ J. 2014. PMID: 24871449 Clinical Trial.
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