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  1. Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2 -developmental encephalopathy
  2. Gain of function due to increased opening probability by two KCNQ5 pore variants causing developmental and epileptic encephalopathy
  3. The Ever Changing Moods of Calmodulin: How Structural Plasticity Entails Transductional Adaptability
  4. Erratum
  5. Neuronal potassium channel openers in the management of epilepsy: role and potential of retigabine