[1P] F. Disorders of the Nervous System 2

[1P-249] Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes

*Koh-ichi Nagata¹, Masashi Nishikawa¹, Hidenori Ito¹ (1. Institute for Developmental Research, Aichi Developmental Disability Center)

Keywords:

RAC3,small GTPase,microcephaly,intellectual disability

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PW: Neuro2022