REPLY: A Distinct Cardiomyopathy HCN4 Syndrome Comprising Myocardial Noncompaction, Bradycardia

Arbustini Eloisa; Favalli Valentina; Narula Nupoor; Serio Alessandra; Grasso Maurizia

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REPLY: A Distinct Cardiomyopathy HCN4 Syndrome Comprising Myocardial Noncompaction, Bradycardia

机译：回复：一种不同的心肌病HCN4综合征，包括心肌非差距，心动过缓

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来源
《Journal of the American College of Cardiology》 |2017年第9期|共3页
作者
Arbustini Eloisa; Favalli Valentina; Narula Nupoor; Serio Alessandra; Grasso Maurizia;
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作者单位

Univ Hosp Policlin San Matteo IRCCS Fdn Ctr Inherited Cardiovasc Dis Piazzale Golgi 19 I-27100;

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原文格式 PDF
正文语种 eng
中图分类心脏、血管（循环系）疾病;
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专利

1. REPLY: A Distinct Cardiomyopathy HCN4 Syndrome Comprising Myocardial Noncompaction, Bradycardia [J] . Arbustini Eloisa, Favalli Valentina, Narula Nupoor, Journal of the American College of Cardiology . 2017,第9期

机译：回复：一种不同的心肌病HCN4综合征，包括心肌非差距，心动过缓
2. HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy [J] . MilanoA., VermeerA.M.C., LodderE.M., Journal of the American College of Cardiology . 2014,第8期

机译：HCN4突变在心动过缓和左心室非紧致性心肌病的多个家庭
3. A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p. [J] . Wessels MW, De-Graaf BM, Cohen-Overbeek TE, Human Genetics . 2008,第6期

机译：伴有非致密性心肌病，心动过缓，肺动脉狭窄，房间隔缺损和异型性的新综合征，提示与6p染色体连锁。
4. Mechanism of Sinus Bradycardia in Carriers of the A414G Mutation in the HCN4 Gene [C] . Arie O. Verkerk, Ronald Wilders Computing in Cardiology Conference . 2019

机译：窦性心动过缓在HCN4基因A414G突变携带者中的作用机制
5. Identification of the gene causing dilated cardiomyopathy with ataxia syndrome (DCMA), a novel Barth syndrome-like condition in the Hutterite population. [D] . Davey, Krista Michelle. 2007

机译：鉴定导致共济失调综合征（DCMA）的扩张性心肌病的基因，DCMA是Hutterite人群中一种新型的Barth综合征样症状。
6. The missense variant p.(Gly482Arg) in HCN4 is responsible for fetal tachy-bradycardia syndrome [O] . Annette Wacker-Gussmann, Renate Oberhoffer-Fritz, Dominik S. Westphal, 2020

机译：HCN4中的错义变体p。（Gly482Arg）导致胎儿心动过缓综合征
7. HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy [O] . Milano, Annalisa, Vermeer, Alexa M. C., Lodder, Elisabeth M., 2014

机译：多家族性心动过缓和左心室非紧密型心肌病的HCN4突变

REPLY: A Distinct Cardiomyopathy HCN4 Syndrome Comprising Myocardial Noncompaction, Bradycardia

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