Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death-Reference-Cited by-同舟云学术

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Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death

Published:2021-01 Issue:1 Volume:23 Page:86-93
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Singer Emma S.,Ross Samantha B.,Skinner Jon R.,Weintraub Robert G.,Ingles Jodie,Semsarian Christopher,Bagnall Richard D.^ORCID

Funder

National Health and Medical Research Council

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

https://www.nature.com/articles/s41436-020-00970-5.pdf

Reference24 articles.

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Protein‐extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregation;Annals of Clinical and Translational Neurology;2024-08-02

2. Clinical Relevance of the Systematic Analysis of Copy Number Variants in the Genetic Study of Cardiomyopathies;Genes;2024-06-13

3. Copy number variations: The potential association genetic cause in severe cardiovascular diseases with unknown aetiology;Journal of Cellular and Molecular Medicine;2024-06

4. Role of Genetics in Diagnosis and Management of Hypertrophic Cardiomyopathy: A Glimpse into the Future;Biomedicines;2024-03-19

5. Analysis of the Association between Copy Number Variation and Ventricular Fibrillation in ST-Elevation Acute Myocardial Infarction;International Journal of Molecular Sciences;2024-02-22

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