Article

Machine Learning Models identify Signature Genes as potential Biomarkers for Hypertrophic Cardiomyopathy from Williams Syndrome

2024-02-29

Abstract excerpt

<title>Abstract</title> <p><bold>Background: </bold>Hypertrophic cardiomyopathy(HCM) is a complex genetic cardiovascular disease with the pathogenesis is still unclear. Williams syndrome(WS), an autosomal dominant systemic disorder with the phenotype of series congenital heart disease that caused by the missing of low-copy DNA elements. The association between the HCM and WS remains unrevealed. This study aimed t...

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Literature Corpus work: 595c838e-5157-5a7a-855c-1080929b07d6
DOI: 10.21203/rs.3.rs-3924392/v1

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