Developmental BiologybioRxivPreprint
Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesis via actomyosin dynamics deregulations
María-Victoria Hinckelmann, Aline Dubos, Victorine Artot…·Yann Hérault
This study shows that Dyrk1a regulates interneuron migration via actomyosin dynamics, leading to cortical GABAergic system defects and phenotypes seen in DYRK1A-haploinsufficiency syndrome.
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