Phenotype and Functional Analyses in a Transgenic Mouse Model of Left Ventricular Noncompaction Caused by a <i>DTNA</i> Mutation-Reference-Cited by-同舟云学术

Phenotype and Functional Analyses in a Transgenic Mouse Model of Left Ventricular Noncompaction Caused by a DTNA Mutation

Published:2017 Issue:6 Volume:58 Page:939-947
ISSN:1349-2365
Container-title:International Heart Journal
language:en
Short-container-title:Int. Heart J.

Author:

Cao Qing¹²,Shen Yang¹,Liu Xin¹,Yu Xin³,Yuan Ping¹,Wan Rong²,Liu Xiuxia²,Peng Xiaogang¹²,He Wenfeng²,Pu Jielin⁴,Hong Kui¹²

Affiliation:

1. Department of Cardiovascular, The Second Affiliated Hospital of Nanchang University

2. The Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University

3. Department of General Surgery, The Second Affiliated Hospital of Nanchang University

4. Fuwai Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College

Publisher

International Heart Journal (Japanese Heart Journal)

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://www.jstage.jst.go.jp/article/ihj/58/6/58_16-019/_pdf

Reference34 articles.

1. 1. Arbustini E, Weidemann F, Hall JL. Left Ventricular noncompaction: a distinct cardiomyopathy or a trait shared by different cardiac diseases? J Am Coll Cardiol 2014; 64: 1840-50.

2. 2. Zipes DP, Camm AJ, Borggrefe M, et al. ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiology Committee for Practice Guidelines (writing committee to develop Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death): developed in collaboration with the European Heart Rhythm Association and the Heart Rhythm Society. Circulation 2006; 114: e385-484.

3. 3. Bione S, D'Adamo P, Maestrini E, Gedeon AK, Bolhuis PA, Toniolo D. A novel X-linked gene, G4.5. is responsible for Barth syndrome. Nat Genet 1996; 12: 385-9.

4. 4. Xing Y, Ichida F, Matsuoka T, et al. Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity. Mol Genet Metab 2006; 88: 71-7.

5. 5. Vatta M, Mohapatra B, Jimenez S, et al. Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction. J Am Coll Cardiol 2003; 42: 2014-27.

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