A Missense Mutation in the CHRM2 Gene Is Associated With Familial Dilated Cardiomyopathy-Reference-Cited by-同舟云学术

A Missense Mutation in the CHRM2 Gene Is Associated With Familial Dilated Cardiomyopathy

Published:2008-06-06 Issue:11 Volume:102 Page:1426-1432
ISSN:0009-7330
Container-title:Circulation Research
language:en
Short-container-title:Circulation Research

Author:

Zhang Lin¹,Hu Aihua¹,Yuan Haixin¹,Cui Liang¹,Miao Guobin¹,Yang Xinchun¹,Wang Lefeng¹,Liu Jinchun¹,Liu Xiulan¹,Wang Shuyan¹,Zhang Zhiyong¹,Liu Lisheng¹,Zhao Rongrui¹,Shen Yan¹

Affiliation:

1. From the Heart Center (L.Z., H.Y., L.C., G.M., X.Y., L.W., J.L., X.L., S.W., Z.Z.), Department of Medicine, Capital Medical University, ChaoYang Hospital, Beijing; Fu Wai Hospital (A.H., L.L.), Chinese Academy of Sciences/Peking Union Medical College, Beijing; Department of Physiology (R.Z.), Shanxi Medical University, Taiyuan; and National Laboratory of Medical Molecular Biology (Y.S.), Institute of Basic Medical Sciences, Chinese Academy of Sciences/Peking Union Medical College, Beijing, China.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

Reference37 articles.

1. Mutation screening of the muscarinic M2 and M3 receptor genes in normal and asthmatic subjects

2. cGMP-mediated inhibition of cardiac L-type Ca2+current by a monoclonal antibody against the M2 ACh receptor

3. Autoimmune myocarditis and dilated cardiomyopathy: focus on cardiac autoantibodies

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