Mutations of Plakophilin-2 in Chinese With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy-Reference-Cited by-同舟云学术

Mutations of Plakophilin-2 in Chinese With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

Published:2009-05 Issue:10 Volume:103 Page:1439-1444
ISSN:0002-9149
Container-title:The American Journal of Cardiology
language:en
Short-container-title:The American Journal of Cardiology

Author:

Qiu Xiaoliang,Liu Wenling,Hu Dayi,Zhu Tiangang,Li Cuilan,Li Lei,Guo Chengjun,Liu Xingpeng,Wang Lei,Zheng Hua,Wang Chunling,Diao Qing,Shi Dan,Zhan Pingyun,Deng Yuanming,Liu Kunshen,Wang Yi,Liu Baomin,Liu Hongming,Zhang Li

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference26 articles.

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2. Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1;Beffagna;Cardiovasc Res,2005

3. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2);Tiso;Hum Mol Genet,2001

4. Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene;Merner;Am J Hum Genet,2008

5. Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease);McKoy;Lancet,2000

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