Associated Papers
Determining the Likelihood of Disease Pathogenicity Among Incidentally Identified Genetic Variants in Rare Dilated Cardiomyopathy-Associated Genes.
Yang Q et al.
Journal of the American Heart Association, 2022
Novel SCN5A p.W697X Nonsense Mutation Segregation in a Family with Brugada Syndrome.
Micaglio E et al.
International Journal of Molecular Sciences, 2019
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