Mechanistic Basis for Type 2 Long QT Syndrome Caused by KCNH2 Mutations that Disrupt Conserved Arginine Residue in the Voltage Sensor

Documenti analoghi

• Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients
  di: Ono, Makoto, et al.
  Pubblicazione: (2020)
• The Cardiomyocyte Molecular Clock Regulates the Circadian Expression of Kcnh2 and Contributes to Ventricular Repolarization
  di: Schroder, Elizabeth A., et al.
  Pubblicazione: (2015)
• Molecular pathogenesis of long QT syndrome type 2
  di: Smith, Jennifer L., et al.
  Pubblicazione: (2016)
• Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulum
  di: Smith, Jennifer L., et al.
  Pubblicazione: (2013)
• Trafficking-deficient hERG K(+) channels linked to long QT syndrome are regulated by a microtubule-dependent quality control compartment in the ER
  di: Smith, Jennifer L., et al.
  Pubblicazione: (2011)