Pathogenic Intronic Splice-Affecting Variants in <i>MYBPC3</i> in Three Patients with Hypertrophic Cardiomyopathy
Genetic variants in <i>MYBPC3</i> are one of the most common causes of hypertrophic cardiomyopathy (HCM). While variants in <i>MYBPC3</i> affecting canonical splice site dinucleotides are a well-characterised cause of HCM, only recently has work begun to investigate the patho...
Hoofdauteurs: | , , , , , , |
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Formaat: | Artikel |
Taal: | English |
Gepubliceerd in: |
MDPI AG
2021-06-01
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Reeks: | Cardiogenetics |
Onderwerpen: | |
Online toegang: | https://www.mdpi.com/2035-8148/11/2/9 |