Jean-Jacques Schott
0000-0002-9578-9475
5 papers found
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Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse
Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome
Cadherin 2-Related Arrhythmogenic Cardiomyopathy
SCN5A Mutation Type and a Genetic Risk Score Associate Variably with Brugada Syndrome Phenotype in SCN5A Families
Primary cilia defects causing mitral valve prolapse
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