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- W8701675 abstract "Aims. We present, for the first time, that loss-of-function mutations in the SCN5A gene encoding for the strong depolarization channel Nav1.5 contribute to SQTS. Methods and Results. We recruited n..." @default.
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- W8701675 date "2012-11-20" @default.
- W8701675 modified "2023-09-23" @default.
- W8701675 title "Abstract 12783: Analysis of SCN5A mutation and Antiarrhythmic Drug in Chinese Patients with Short QT Syndrome" @default.
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