[2LBA] Late-Breaking Abstracts

[2LBA-003] A deficiency of Girdin in Nkx2-1-lineage interneurons generates intractable epilepsy

*Machiko Iida¹, Motoki Tanaka¹, Naoya Asai², Masahide Takahashi², Masato Asai^1,2 (1. Institute For Developmental Research, Aichi Developmental Disability Center, Aichi, Japan, 2. Nagoya Univ Grad Sch of Med, Nagoya, Japan)

Keywords:Girdin/ccdc88a, Developmental and epileptic encephalopathies, Mesial temporal lobe epilepsy, Migration defects of interneuron