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Updated: Nov 6, 2025

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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A novel familial SCN5A exon 20 deletion is associated with a heterogeneous phenotype

Utkarsh Kohli1, Chenni S Sriram2, Hemal M Nayak3

  • 1Division of Pediatric Cardiology, Department of Pediatrics, Comer Children's Hospital and the Pritzker School of Medicine of the University of Chicago, Chicago, IL, USA; Division of Pediatric Cardiology/Electrophysiology, Department of Pediatrics, West Virginia School of Medicine, Morgantown, WV, USA.

Journal of Electrocardiology
|May 5, 2021
PubMed

Keywords:
Atrial fibrillationBrugada ECG patternSCN5A exon 20 deletion (c.3667-?_c.3840C +?del)Sinus node dysfunction

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