Rare compound heterozygous missense SPATA7 variations and risk of schizophrenia; whole-exome sequencing in a consanguineous family with affected siblings, follow-up sequencing and...

por Igeta, Hirofumi, Watanabe, Yuichiro, Morikawa, Ryo, Ikeda, Masashi, Otsuka, Ikuo, Hoya, Satoshi, Koizumi, Masataka, Egawa, Jun, Hishimoto, Akitoyo, Iwata, Nakao, Someya, Toshiyuki
Publicado 2019

Novel Rare Missense Variations and Risk of Autism Spectrum Disorder: Whole-Exome Sequencing in Two Families with Affected Siblings and a Two-Stage Follow-Up Study in a Japanese Pop...

por Egawa, Jun, Watanabe, Yuichiro, Wang, Chenyao, Inoue, Emiko, Sugimoto, Atsunori, Sugiyama, Toshiro, Igeta, Hirofumi, Nunokawa, Ayako, Shibuya, Masako, Kushima, Itaru, Orime, Naoki, Hayashi, Taketsugu, Okada, Takashi, Uno, Yota, Ozaki, Norio, Someya, Toshiyuki
Publicado 2015

Resequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese Population

por Inoue, Emiko, Watanabe, Yuichiro, Xing, Jingrui, Kushima, Itaru, Egawa, Jun, Okuda, Shujiro, Hoya, Satoshi, Okada, Takashi, Uno, Yota, Ishizuka, Kanako, Sugimoto, Atsunori, Igeta, Hirofumi, Nunokawa, Ayako, Sugiyama, Toshiro, Ozaki, Norio, Someya, Toshiyuki
Publicado 2015