Presentation Information

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

*Machiko Iida1, Motoki Tanaka1, Naoya Asai2, Masahide Takahashi2, Masato Asai1,2 (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

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PW: Neuro2022