Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family

Lignende værker

• Jervell and Lange-Nielsen syndrome (case report) Jervell and Lange-Nielsen syndrome (prolonged QT interval and hearing loss)
  af: Ali A.-A. Mohammad Al-Mousawi, et al.
  Udgivet: (2016-04-01)
• Mutational and Phenotypic Spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome
  af: Faridi, Rabia, et al.
  Udgivet: (2018)
• Jervell and Lange-Nielsen syndrome with novel KCNQ1 and additional gene mutations
  af: Matsuda, Shinichi, et al.
  Udgivet: (2020)
• Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias.
  af: Chouabe, C, et al.
  Udgivet: (1997)
• Large Deletion in KCNQ1 Identified in a Family with Jervell and Lange-Nielsen Syndrome
  af: Sung, Ji Yeon, et al.
  Udgivet: (2014)