Novel Phenotypic Effects of a Rare SCN5A (c.2482C>T) Mutation
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Publisher
Elsevier BV
Reference12 articles.
1. SCN5A variants: association with cardiac disorders;Li;Front Physiol,2018
2. Clinical spectrum of SCN5A mutations: long QT syndrome, Brugada syndrome, and cardiomyopathy;Wilde;J Am Coll Cardiol EP,2018
3. A novel familial SCN5A exon 20 deletion is associated with a heterogeneous phenotype;Kohli;J Electrocardiol,2021
4. Beauty and the beat: a complicated case of multifocal ectopic Purkinje-related premature contractions;Ter Bekke;HeartRhythm Case Rep,2018
5. Prognostic relevance of gene-environment interactions in patients with dilated cardiomyopathy: applying the MOGE(S) classification;Hazebroek;J Am Coll Cardiol,2015
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