An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene SCN4A

Lignende værker

• Familial hyperkalemic periodic paralysis caused by a de novo mutation in the sodium channel gene SCN4A
  af: Han, Ji-Yeon, et al.
  Udgivet: (2011)
• Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current
  af: Jurkat-Rott, Karin, et al.
  Udgivet: (2000)
• The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis
  af: Kim, June-Bum, et al.
  Udgivet: (2007)
• A Korean Family of Hypokalemic Periodic Paralysis with Mutation in a Voltage-gated Calcium Channel (R1239G)
  af: Kim, June-Bum, et al.
  Udgivet: (2005)
• Mutations in Potassium Channel Kir2.6 Cause Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis
  af: Ryan, Devon P., et al.
  Udgivet: (2010)