Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes

Koh-ichi Nagata

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

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

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