Correction: Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients

Eitemau Tebyg

• Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients
  gan: Ohno, Seiko, et al.
  Cyhoeddwyd: (2015)
• Bradycardia Is a Specific Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia Induced by RYR2 Mutations
  gan: Miyata, Kazuaki, et al.
  Cyhoeddwyd: (2018)
• Identification of a novel exon3 deletion of RYR2 in a family with catecholaminergic polymorphic ventricular tachycardia
  gan: Dharmawan, Tommy, et al.
  Cyhoeddwyd: (2019)
• In Vivo Ryr2 Editing Corrects Catecholaminergic Polymorphic Ventricular Tachycardia
  gan: Pan, Xiaolu, et al.
  Cyhoeddwyd: (2018)
• Three cases of catecholaminergic polymorphic ventricular tachycardia with prolonged QT intervals including two cases of compound mutations
  gan: Saito, Aki, et al.
  Cyhoeddwyd: (2018)