Genetic KCa3.1-deficiency produces locomotor hyperactivity and alterations in cerebral monoamine levels.

by Kate Lykke Lambertsen, Jan Bert Gramsbergen, Mithula Sivasaravanaparan, Nicholas Ditzel, Linda Maria Sevelsted-Møller, Aida Oliván-Viguera, Maj Rabjerg, Heike Wulff, Ralf Köhler
Published 2012-01-01