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A novel familial SCN5A exon 20 deletion is associated with a heterogeneous phenotype.
Kohli U, Sriram CS, Nayak HM. A novel familial SCN5A exon 20 deletion is associated with a heterogeneous phenotype. J Electrocardiol. 2021 May-Jun; 66:131-135.
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PubMed
subject areas
Brugada Syndrome
Electrocardiography
Exons
Humans
Mutation
Phenotype
authors with profiles
Utkarsh Kohli
Hemal Nayak
A novel familial SCN5A exon 20 deletion is associated with a heterogeneous phenotype.