Idiopathic ventricular fibrillation and the V1764fsX1786 frameshift mutation of the SCN5A gene in a myotonic dystrophy type 1 patient-Reference-Cited by-同舟云学术

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Idiopathic ventricular fibrillation and the V1764fsX1786 frameshift mutation of the SCN5A gene in a myotonic dystrophy type 1 patient

Published:2020-04 Issue: Volume:74 Page:242-244
ISSN:0967-5868
Container-title:Journal of Clinical Neuroscience
language:en
Short-container-title:Journal of Clinical Neuroscience

Author:

Shimoyama Takashi,Hayashi Hiroshi,Suzuki Fumiaki,Nishiyama Yasuhiro,Miyamoto Yoshihiro,Aiba Takeshi,Shimizu Wataru,Kimura Kazumi

Publisher

Elsevier BV

Subject

Physiology (medical),Clinical Neurology,Neurology,General Medicine,Surgery

Reference9 articles.

1. Myotonic dystrophymutation: an unstable CTG repeat in the 3′ untranslated region of the gene;Mahadevan;Science,1992

2. Electrocardiographic abnor-malities and sudden death in myotonic dystrophy type 1;Groh;N Engl J Med,2008

3. Risk of arrhythmia in type I myotonic dystrophy: the role of clinical and genetic variables;Cudia;J Neurol Neurosurg Psychiatry,2009

4. Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1;Wahbi;Arch Cardiovasc Dis,2013

5. Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation;Pambrun;Heart Rhythm,2014

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Arrhythmias and Conduction System Disease;Disorders of the Heart and Blood Vessels;2023-11-15

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