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  • Michael G Leitner, Anja Feuer, Olga Ebers, Daniela N. Schreiber, Christian R. Halaszovich, Dominik Oliver
  • Chemistry, Medicine
  • British journal of pharmacology
  • 2012 (First Publication: 1 April 2012)
  • BACKGROUND AND PURPOSE DFNA2 is a frequent hereditary hearing disorder caused by loss-of-function mutations in the voltage-gated potassium channel KCNQ4 (Kv7.4). KCNQ4 mediates the predominant K(+)Expand