Disease-causing mutations C277R and C277Y modify gating of human ClC-1 chloride channels in myotonia congenita

Lignende værker

• ClC1 chloride channel in myotonic dystrophy type 2 and ClC1 splicing in vitro
  af: URSU, SIMONA-FELICIA, et al.
  Udgivet: (2012)
• The Myotonia Congenita Mutation A331T Confers a Novel Hyperpolarization-Activated Gate to the Muscle Chloride Channel ClC-1
  af: Warnstedt, Maike, et al.
  Udgivet: (2002)
• Multimeric structure of ClC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen).
  af: Steinmeyer, K, et al.
  Udgivet: (1994)
• Defective Gating and Proteostasis of Human ClC-1 Chloride Channel: Molecular Pathophysiology of Myotonia Congenita
  af: Jeng, Chung-Jiuan, et al.
  Udgivet: (2020)
• Activation of renal ClC-K chloride channels depends on an intact N terminus of their accessory subunit barttin
  af: Wojciechowski, Daniel, et al.
  Udgivet: (2018)