[3P] 16 Neurogenesis and Gliogenesis

[3P-056] Elucidating the pathogenic mechanism of Seckel syndrome caused by the interaction and functional disruption of centrosomal proteins CEP152 and PLK4

*Nanako Hamada¹, Ikuko Iwamoto¹, Koh-ichi Nagata¹ (1. Inst for Dev Res, Aichi Dev Disability Center, )

Keywords:CEP152, microcephaly, centrosome, dendrite development