High-degree atrioventricular block revealing hypertrophic cardiomyopathy related to a mutation in MYBPC3 gene

Kouakam Claude; Boule Stephane; Brigadeau Francois

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High-degree atrioventricular block revealing hypertrophic cardiomyopathy related to a mutation in MYBPC3 gene

机译：高度房室间块，揭示与myBPC3基因突变相关的肥厚性心肌病

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来源
《La Presse medicale》 |2019年第1期|共4页
作者
Kouakam Claude; Boule Stephane; Brigadeau Francois;
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作者单位

Lille Univ Hosp Dept Cardiol F-59037 Lille France;

Lille Univ Hosp Dept Cardiol F-59037 Lille France;

Lille Univ Hosp Dept Cardiol F-59037 Lille France;

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原文格式 PDF
正文语种 eng
中图分类外科学;
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专利

1. High-degree atrioventricular block revealing hypertrophic cardiomyopathy related to a mutation in MYBPC3 gene [J] . Kouakam Claude, Boule Stephane, Brigadeau Francois La Presse medicale . 2019,第1期

机译：高度房室间块，揭示与myBPC3基因突变相关的肥厚性心肌病
2. Next-generation sequencing (NGS) as a molecular diagnostic tool for hypertrophic cardiomyopathy in a Chinese boy due to novel compound heterozygous mutations in the MYBPC3 gene: A case report [J] . Chen Xu, Jiang Jun, Zhu Weiliang, Medicine. . 2019,第12期

机译：新一代测序（NGS）作为中国男孩肥大型心肌病的分子诊断工具，原因是MYBPC3基因中出现了新的复合杂合突变：一例
3. 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 [J] . CamugliaA.C., YoungerJ.F., McGaughranJ., International Journal of Cardiology . 2013,第3期

机译：心肌肌球蛋白结合蛋白C基因突变在两个家族中表现为肥厚型心肌病和左心室不紧致：心脏磁共振的临床筛查见识：Camuglia MYBPC3基因突变和MRI
4. Apical Hypertrophic Cardiomyopathy with a rare MYBPC3 gene mutation variant [C] . Ahmad T.A., Bhattacharya P., Al-bataineh M. World Congress on Heart Disease . 2012

机译：具有罕见的MyBPC3基因突变变体的顶端肥厚性心肌病
5. Physiologic Studies of Familial Hypertrophic Cardiomyopathy-Related Mutations in Cardiac Troponin T. [D] . Jimenez, Jesus. 2013

机译：心肌肌钙蛋白T中家族性肥厚性心肌病相关突变的生理研究。
6. Prevalence and Phenotypic Expression of Mutations in theMYH7 MYBPC3 and TNNT2 Genes in Familieswith Hypertrophic Cardiomyopathy in the South of Brazil: A Cross-SectionalStudy [O] . Beatriz Piva e Mattos, Fernando Luís Scolari, Marco Antonio Rodrigues Torres, 2016

机译：流行和表型表达的突变家庭中的MYH7MYBPC3和TNNT2基因南部的肥厚型心肌病患者：跨部门研究
7. Next-generation sequencing (NGS) as a molecular diagnostic tool for hypertrophic cardiomyopathy in a Chinese boy due to novel compound heterozygous mutations in the MYBPC3 gene [O] . Xu Chen, Jun Jiang, Weiliang Zhu, 2019

机译：由于新型化合物杂合子突变在MYBPC3基因中，下一代测序（NGS）作为一种中国男孩的分子诊断工具

High-degree atrioventricular block revealing hypertrophic cardiomyopathy related to a mutation in MYBPC3 gene

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