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

24 Sept 2020

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Share to Cardiac electrophysiology and arrhythmias
Share to Congenital heart defects research
Share to Genomic variations and chromosomal abnormalities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 32973354
DOI: 10.1038/s41436-020-00970-5

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