Literature DB >> 23739544

Role of mutations in L-type calcium channel genes in Brugada syndrome, early repolarization syndrome, and idiopathic ventricular fibrillation associated with right bundle branch block.

Hiroshi Watanabe, Tohru Minamino.   

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Year:  2013        PMID： 23739544     DOI： 10.1253/circj.cj-13-0641

Source DB:  PubMed          Journal:  Circ J        ISSN： 1346-9843            Impact factor:   2.993


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  2 in total

Review 1.  The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance.

Authors:  Jean-Baptiste Gourraud; Julien Barc; Aurélie Thollet; Solena Le Scouarnec; Hervé Le Marec; Jean-Jacques Schott; Richard Redon; Vincent Probst
Journal:  Front Cardiovasc Med       Date:  2016-04-25

2.  SCN1Bβ mutations that affect their association with Kv4.3 underlie early repolarization syndrome.

Authors:  Hao Yao; Jun Fan; Yun-Jiu Cheng; Xu-Miao Chen; Cheng-Cheng Ji; Li-Juan Liu; Zi-Heng Zheng; Su-Hua Wu
Journal:  J Cell Mol Med       Date:  2018-08-30       Impact factor: 5.310
  2 in total

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