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4. CDKL5 protein substitution therapy rescues neurological phenotypes of a mouse model of CDKL5 disorder. (20th February 2018)

5. Heterozygous CDKL5 Knockout Female Mice Are a Valuable Animal Model for CDKL5 Disorder. (27th May 2018)

9. Physiological time structure of the tibialis anterior motor activity during sleep in mice, rats and humans. (25th June 2015)