Hiraide, T., Hattori, A., Ieda, D., Hori, I., Saitoh, S., Nakashima, M., & Saitsu, H. (2019). De novo variants in SETD1B cause intellectual disability, autism spectrum disorder, and epilepsy with myoclonic absences. Epilepsia Open.

Hiraide, Takuya, Ayako Hattori, Daisuke Ieda, Ikumi Hori, Shinji Saitoh, Mitsuko Nakashima, و Hirotomo Saitsu. "De Novo Variants in SETD1B Cause Intellectual Disability, Autism Spectrum Disorder, and Epilepsy With Myoclonic Absences." Epilepsia Open 2019.

Hiraide, Takuya, et al. "De Novo Variants in SETD1B Cause Intellectual Disability, Autism Spectrum Disorder, and Epilepsy With Myoclonic Absences." Epilepsia Open 2019.