Literature DB >> 23642604

Cardiac myosin-binding protein C gene mutation expressed as hypertrophic cardiomyopathy and left ventricular noncompaction within two families: insights from cardiac magnetic resonance in clinical screening: Camuglia MYBPC3 gene mutation and MRI.

Anthony C Camuglia1, John F Younger, Julie McGaughran, Ada Lo, John J Atherton.   

Abstract

Entities:  

Keywords:  Cardiomyopathy; Genetic heart disease; Magnetic resonance imaging; Screening

Mesh：

Substances：

Year:  2013        PMID： 23642604     DOI： 10.1016/j.ijcard.2013.03.168

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN： 0167-5273            Impact factor:   4.164


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  3 in total

1.  Overlap phenotypes of the left ventricular noncompaction and hypertrophic cardiomyopathy with complex arrhythmias and heart failure induced by the novel truncated DSC2 mutation.

Authors:  Yubi Lin; Jiana Huang; Zhiling Zhu; Zuoquan Zhang; Jianzhong Xian; Zhe Yang; Tingfeng Qin; Linxi Chen; Jingmin Huang; Yin Huang; Qiaoyun Wu; Zhenyu Hu; Xiufang Lin; Geyang Xu
Journal:  Orphanet J Rare Dis       Date:  2021-11-24       Impact factor: 4.123

2.  Left Ventricular Noncompaction Is Associated with Valvular Regurgitation and a Variety of Arrhythmias.

Authors:  Qing Li; Lianjie Miao; Lihong Xia; Hala Y Abdelnasser; Fang Zhang; Yangyang Lu; Anika Nusrat; Mantasha Tabassum; Juxiang Li; Mingfu Wu
Journal:  J Cardiovasc Dev Dis       Date:  2022-02-02

3.  Family screening in black patients with isolated left ventricular non-compaction: the Chris Hani Baragwanath experience.

Authors:  Anneen L Basson; Mohammed R Essop; Elena Libhaber; Ferande Peters
Journal:  Cardiovasc J Afr       Date:  2020-03-11       Impact factor: 1.167
  3 in total

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