ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy-Reference-Cited by-同舟云学术

ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy

Published:2018-02-14 Issue:7 Volume:33 Page:722-732
ISSN:0910-8327
Container-title:Heart and Vessels
language:en
Short-container-title:Heart Vessels

Author:

Sun Yu-Min,Wang Jun,Xu Ying-Jia,Wang Xin-Hua,Yuan Fang,Liu Hua,Li Ruo-Gu,Zhang Min,Li Yan-Jie,Shi Hong-Yu,Zhao Liang,Qiu Xing-Biao,Qu Xin-Kai,Yang Yi-Qing

Funder

The National Natural Science Foundation of China

The Key Program for Basic Research of Shanghai, China

The Natural Science Foundation of Shanghai, China

The Experimental Animal Program of Shanghai, China

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine

Link

http://link.springer.com/article/10.1007/s00380-017-1110-4/fulltext.html

Reference54 articles.

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3. Elliott P, Charron P, Blanes JR, Tavazzi L, Tendera M, Konté M, Laroche C, Maggioni AP, EORP Cardiomyopathy Registry Pilot Investigators (2016) European Cardiomyopathy Pilot Registry: EURObservational Research Programme of the European Society of Cardiology. Eur Heart J 37:164–173

4. Yagishita-Tagawa Y, Abe Y, Arai K, Yagishita D, Takagi A, Ashihara K, Shoda M, Naruko T, Itoh A, Haze K, Yoshikawa J, Hagiwara N (2013) Low-dose dobutamine induces left ventricular mechanical dyssynchrony in patients with dilated cardiomyopathy and a narrow QRS: a study using real-time three-dimensional echocardiography. J Cardiol 61:275–280

5. Takahashi A, Shiga T, Shoda M, Tanizaki K, Manaka T, Ejima K, Kasanuki H, Hagiwara N (2010) Gender difference in arrhythmic occurrences in patients with nonischemic dilated cardiomyopathy and implantable cardioverter-defibrillator. Heart Vessels 25:150–154

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