[2S06a] Connecting dots of CNV-linked structural and functional phenotypes from humans to mice

[2S06a-5] TBX1, a gene encoded in 22q11.2 copy number variation, contributes to structural, cellular, and behavioral deficits via neonatal and embryonic neurogenesis

*Noboru Hiroi¹, Takeshi Hiramoto¹, Shuken Boku², Akira Sumiyoshi^4,3, Risa Kato⁵, Takahira Yamauchi¹, Takeshi Takano¹, Emily T. Averyt¹, Takaki Tanifuji¹, Gina Kang¹, Marisa Esparza¹, Yukiko J Hiroi¹, Rie Ryoke³, Hiroi Nonaka³, Akihiro Machida⁵, Kensaku Nomoto⁵, Kazutaka Mogi⁵, Takefumi Kikusui⁵, Ryuta Kawashima³, Jason Pugh¹ (1. UT Health San Antonio, San Antonio, USA, 2. Kumamoto University, Kumamoto, Japan, 3. Tohoku University, Miyagi, Japan, 4. NIRS-QST, Chiba, Japan, 5. Azabu University, Kanagawa, Japan)

キーワード：

CNV、social behavior、stem cell、neurodevelopmental disorders

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