Letter by Perez-Riera et al Regarding Article, 'Left-Dominant Arrhythmogenic Cardiomyopathy With Heterozygous Mutations in DSP and MYBPC3'

Perez-Riera Andres Ricardo; Barbosa-Barros Raimundo; Belhassen Bernard

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Letter by Perez-Riera et al Regarding Article, 'Left-Dominant Arrhythmogenic Cardiomyopathy With Heterozygous Mutations in DSP and MYBPC3'

机译：Perez-Riera等人关于文章的信，“左派致力致血管生成症与DSP和MyBPC3中的杂合酶突变”

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来源
《Circulation. Cardiovascular imaging》 |2019年第9期|共2页
作者
Perez-Riera Andres Ricardo; Barbosa-Barros Raimundo; Belhassen Bernard;
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作者单位

Fac Med ABC Lab Metodol Pesquisa &

Escrita Cient Santo Andre SP Brazil;

Hosp Messejana Dr Carlos Alberto Studart Gomes Coronary Ctr Fortaleza Ceara Brazil;

Hadassah Univ Hosp Heart Inst Jerusalem Israel;

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原文格式 PDF
正文语种 eng
中图分类诊断学;
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1. Letter by Perez-Riera et al Regarding Article, "Left-Dominant Arrhythmogenic Cardiomyopathy With Heterozygous Mutations in DSP and MYBPC3" [J] . Perez-Riera Andres Ricardo, Barbosa-Barros Raimundo, Belhassen Bernard Circulation. Cardiovascular imaging . 2019,第9期

机译：Perez-Riera等人关于文章的信，“左派致力致血管生成症与DSP和MyBPC3中的杂合酶突变”
2. Left-Dominant Arrhythmogenic Cardiomyopathy With Heterozygous Mutations in DSP and MYBPC3 [J] . Sakamoto Naka, Natori Shunsuke, Hosoguchi Shohei, Circulation. Cardiovascular imaging . 2019,第6期

机译：左侧占血小性心肌病变，杂合酶突变在DSP和MYBPC3中
3. Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects [J] . Wessels Marja W., Herkert Johanna C., Frohn-Mulder Ingrid M., European journal of human genetics: EJHG . 2015,第7期

机译：复合杂合或纯合截短的MYBPC3突变会导致致命的心肌病，具有非致密性和间隔缺损
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. A Multi-Scale Computational Approach to Understand the Calcium Dynamics and Arrhythmogenic Disorders Caused by Mutations in RYR2/CASQ2 Expressing Genes [D] . Paudel, Roshan. 2020

机译：一种多规模的计算方法，了解Ryr2 / Casq2在表达基因中突变引起的钙动力学和心律发生障碍
6. Response by Sakamoto et al to Letter Regarding Article Left-Dominant Arrhythmogenic Cardiomyopathy With Heterozygous Mutations in DSP and MYBPC3 [O] . Naka Sakamoto, Shunsuke Natori, Shohei Hosoguchi, -1

机译：Sakamoto等人对信函的回复： DSP和MYBPC3中具有杂合突变的左占主导性心律失常性心肌病
7. Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects [O] . Wessels, M.W. (Marja), Herkert, J.C. (Johanna), Frohn-Mulder, I.M.E. (Ingrid), 2015

机译：复合杂合或纯合截断MYBPC3突变会导致致命的心肌病，其特征为非致密性和间隔缺损

Letter by Perez-Riera et al Regarding Article, 'Left-Dominant Arrhythmogenic Cardiomyopathy With Heterozygous Mutations in DSP and MYBPC3'

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