Benign Familial Neonatal Convulsions Caused by Altered Gating of KCNQ2/KCNQ3 Potassium Channels

פריטים דומים

• Atypical Gating Of M-Type Potassium Channels Conferred by Mutations in Uncharged Residues in the S(4) Region of KCNQ2 Causing Benign Familial Neonatal Convulsions
  מאת: Soldovieri, Maria Virginia, et al.
  יצא לאור: (2007)
• M Channels Containing KCNQ2 Subunits Modulate Norepinephrine, Aspartate, and GABA Release from Hippocampal Nerve Terminals
  מאת: Martire, Maria, et al.
  יצא לאור: (2004)
• Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsions
  מאת: Concolino, D, et al.
  יצא לאור: (2002)
• Two Novel KCNQ2 Mutations in 2 Families With Benign Familial Neonatal Convulsions
  מאת: Al Yazidi, Ghalia, et al.
  יצא לאור: (2017)
• The First Korean Case of KCNQ2 Mutation in a Family with Benign Familial Neonatal Convulsions
  מאת: Yum, Mi-Sun, et al.
  יצא לאור: (2010)