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本文引用的文献

1
Reevaluation of the South Asian Intronic Deletion in Hypertrophic Cardiomyopathy.肥厚型心肌病中南亚内含子缺失的再评估。
Circ Genom Precis Med. 2020 Jun;13(3):e002783. doi: 10.1161/CIRCGEN.119.002783. Epub 2020 Mar 12.
2
Designing Human In Vitro Models for Drug Development.为药物研发设计人体体外模型。
J Am Coll Cardiol. 2020 Feb 18;75(6):587-589. doi: 10.1016/j.jacc.2019.12.013.
3
Myosin binding protein-C and hypertrophic cardiomyopathy: role of altered C10 domain.肌球蛋白结合蛋白-C与肥厚型心肌病：C10结构域改变的作用
Cardiovasc Res. 2019 Dec 1;115(14):1943-1945. doi: 10.1093/cvr/cvz167.
4
Altered C10 domain in cardiac myosin binding protein-C results in hypertrophic cardiomyopathy.心肌肌球蛋白结合蛋白 C 的 C10 结构域改变导致肥厚型心肌病。
Cardiovasc Res. 2019 Dec 1;115(14):1986-1997. doi: 10.1093/cvr/cvz111.
5
Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy.全基因组测序可改善肥厚型心肌病患者基因检测的结果。
J Am Coll Cardiol. 2018 Jul 24;72(4):419-429. doi: 10.1016/j.jacc.2018.04.078.
6
Atherosclerotic Cardiovascular Disease in South Asians in the United States: Epidemiology, Risk Factors, and Treatments: A Scientific Statement From the American Heart Association.美国南亚裔人群的动脉粥样硬化性心血管疾病：流行病学、风险因素和治疗：美国心脏协会的科学声明。
Circulation. 2018 Jul 3;138(1):e1-e34. doi: 10.1161/CIR.0000000000000580. Epub 2018 May 24.
7
Association of Cardiomyopathy With MYBPC3 D389V and MYBPC3Δ25bpIntronic Deletion in South Asian Descendants.南亚裔人群中心肌病与 MYBPC3 D389V 和 MYBPC3Δ25bp 内含子缺失的相关性。
JAMA Cardiol. 2018 Jun 1;3(6):481-488. doi: 10.1001/jamacardio.2018.0618.
8
India's March to Halt the Emerging Cardiovascular Epidemic.印度遏制心血管疾病新流行的行动
Circ Res. 2017 Sep 29;121(8):913-916. doi: 10.1161/CIRCRESAHA.117.310904.
9
Role of common sarcomeric gene polymorphisms in genetic susceptibility to left ventricular dysfunction.常见肌节基因多态性在左心室功能障碍遗传易感性中的作用。
J Genet. 2016 Jun;95(2):263-72. doi: 10.1007/s12041-016-0623-4.
10
The Incidence of Major Cardiovascular Events in Immigrants to Ontario, Canada: The CANHEART Immigrant Study.加拿大安大略省移民中主要心血管事件的发生率：加拿大心脏移民研究
Circulation. 2015 Oct 20;132(16):1549–1559. doi: 10.1161/CIRCULATIONAHA.115.015345. Epub 2015 Aug 31.

South Asian-Specific Intronic Deletion and Its Role in Cardiomyopathies and Heart Failure.

作者信息

Sadayappan Sakthivel, Puckelwartz Megan J, McNally Elizabeth M

机构信息

Division of Cardiovascular Health and Disease, Department of Internal Medicine, Heart, Lung and Vascular Institute, College of Medicine, University of Cincinnati, OH. Center for Genetic Medicine, Northwestern University, Chicago, IL.

出版信息

Circ Genom Precis Med. 2020 Jun;13(3):e002986. doi: 10.1161/CIRCGEN.120.002986. Epub 2020 Jun 16.

DOI:10.1161/CIRCGEN.120.002986
PMID:32543992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7301913/
Abstract
摘要