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Neuronal defects in a human cellular model of 22q11.2 deletion syndrome
Khan, Themasap A., Revah, Omer, Gordon, Aaron, Yoon, Se-Jin, Krawisz, Anna K., Goold, Carleton, Sun, Yishan, Kim, Chul Hoon, Tian, Yuan, Li, Min-Yin, Schaepe, Julia M., Ikeda, Kazuya, Amin, Neal D., Sakai, Noriaki, Yazawa, Masayuki, Kushan, Leila, Nishino, Seiji, Porteus, Matthew H., Rapoport, Judith L., Bernstein, Jonathan A., O’Hara, Ruth, Bearden, Carrie E., Hallmayer, Joachim F., Huguenard, John R., Geschwind, Daniel H., Dolmetsch, Ricardo E., Paşca, Sergiu P.
Published in Nature medicine (01.12.2020)
Published in Nature medicine (01.12.2020)
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