High Risk for Bradyarrhythmic Complications in Patients With Brugada Syndrome Caused by SCN5AGene Mutations-Reference-Cited by-同舟云学术

High Risk for Bradyarrhythmic Complications in Patients With Brugada Syndrome Caused by SCN5AGene Mutations

Published:2005-12 Issue:11 Volume:46 Page:2100-2106
ISSN:0735-1097
Container-title:Journal of the American College of Cardiology
language:en
Short-container-title:Journal of the American College of Cardiology

Author:

Makiyama Takeru,Akao Masaharu,Tsuji Keiko,Doi Takahiro,Ohno Seiko,Takenaka Kotoe,Kobori Atsushi,Ninomiya Tomonori,Yoshida Hidetada,Takano Makoto,Makita Naomasa,Yanagisawa Fumiko,Higashi Yukei,Takeyama Youichi,Kita Toru,Horie Minoru

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

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3. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation;Chen;Nature,1998

4. Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome;Priori;Circulation,2000

5. The Brugada syndrome;Antzelevitch;J Cardiovasc Electrophysiol,2001

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