β-肌球蛋白重链变异体引起的儿童肥厚型心肌病与肌球蛋白结合蛋白C疾病相比具有更大的阻塞性但较少的致心律失常表型有关。

IF 6 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Circulation: Genomic and Precision Medicine Pub Date : 2023-10-01 Epub Date: 2023-06-30 DOI:10.1161/CIRCGEN.123.004118
Gabrielle Norrish, Vidthya Kadirrajah, Ella Field, Kathleen Dady, Jennifer Tollit, Karen McLeod, Ruth McGowan, Elena Cervi, Juan Pablo Kaski
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Childhood Hypertrophic Cardiomyopathy Caused by Beta-Myosin Heavy Chain Variants Is Associated With a More Obstructive but Less Arrhythmogenic Phenotype Than Myosin-Binding Protein C Disease.
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来源期刊
Circulation: Genomic and Precision Medicine
Circulation: Genomic and Precision Medicine Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
9.20
自引率
5.40%
发文量
144
期刊介绍: Circulation: Genomic and Precision Medicine is a distinguished journal dedicated to advancing the frontiers of cardiovascular genomics and precision medicine. It publishes a diverse array of original research articles that delve into the genetic and molecular underpinnings of cardiovascular diseases. The journal's scope is broad, encompassing studies from human subjects to laboratory models, and from in vitro experiments to computational simulations. Circulation: Genomic and Precision Medicine is committed to publishing studies that have direct relevance to human cardiovascular biology and disease, with the ultimate goal of improving patient care and outcomes. The journal serves as a platform for researchers to share their groundbreaking work, fostering collaboration and innovation in the field of cardiovascular genomics and precision medicine.
期刊最新文献
Patient Perceptions of Emerging Gene Therapies for Arrhythmogenic Right Ventricular Cardiomyopathy. Polygenic Prediction of Recurrent Events After Early-Onset Myocardial Infarction. Understanding the Complex Genetics of Spontaneous Coronary Artery Dissection: A Guide for Clinicians. Sex-Specific Association Between Genetic Risk of Psychiatric Disorders and Cardiovascular Diseases. Cardiovascular Disease Pathogenicity Predictor (CVD-PP): A Tissue-Specific In Silico Tool for Discriminating Pathogenicity of Variants of Unknown Significance in Cardiovascular Disease Genes.
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