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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
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