IRX3 variant as a modifier of Brugada syndrome with frequent ventricular fibrillation

HeartRhythm Case Rep. 2016 Aug 2;2(6):465-468. doi: 10.1016/j.hrcr.2016.06.002. eCollection 2016 Nov.

Yoshitaka Kimura^{1

2}, Takeshi Aiba¹, Tetsuo Sasano³, Tetsushi Furukawa⁴, Kengo Kusano¹, Wataru Shimizu^{1

5}

¹ Division of Arrhythmia and Electrophysiology, Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan.
² Department of Advanced Cardiovascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
³ Department of Biofunctional Informatics, Tokyo Medical and Dental University, Tokyo, Japan.
⁴ Department of Bio-Informational Pharmacology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
⁵ Department of Cardiovascular Medicine, Nippon Medical School, Tokyo, Japan.

No abstract available

Keywords: Brugada syndrome; Genes; IRX3; SCN5A; Ventricular fibrillation.

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