Enhanced impact of SCN5A mutation associated with long QT syndrome in fetal splice isoform

Ítems similars

• Mutational analysis of SCN5A gene in long QT syndrome
  per: Qureshi, Sameera Fatima, et al.
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• A case of long QT syndrome having compound mutations of KCNH2 and SCN5A
  per: Ito, Saki, et al.
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• CRISPR‐Mediated Expression of the Fetal Scn5a Isoform in Adult Mice Causes Conduction Defects and Arrhythmias
  per: Pang, Paul D., et al.
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• Long QT Syndrome–Associated Mutations in Intrauterine Fetal Death
  per: Crotti, Lia, et al.
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• Normalization of Ventricular Repolarization with Flecainide in Long QT Syndrome Patients with SCN5A:ΔKPQ Mutation
  per: Windle, John R., et al.
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