Progressive myoclonus epilepsy KCNC1 (KV3.1) variant causes a developmental dendritopathy.
A novel role of CDKL5 at inhibitory synapses and a possible therapeutic strategy for CDKL5-related defects.
Inhibiting microcephaly genes as alternative to microtubule targeting agents to treat brain tumors.
Modelling focal cortical dysplasia by driving PTEN gene deletion with a novel Cre-amplifying reporter.
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