CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate

por Suzuki, Toshimitsu, Tatsukawa, Tetsuya, Sudo, Genki, Delandre, Caroline, Pai, Yun Jin, Miyamoto, Hiroyuki, Raveau, Matthieu, Shimohata, Atsushi, Ohmori, Iori, Hamano, Shin-ichiro, Haginoya, Kazuhiro, Uematsu, Mitsugu, Takahashi, Yukitoshi, Morimoto, Masafumi, Fujimoto, Shinji, Osaka, Hitoshi, Oguni, Hirokazu, Osawa, Makiko, Ishii, Atsushi, Hirose, Shinichi, Kaneko, Sunao, Inoue, Yushi, Moore, Adrian Walton, Yamakawa, Kazuhiro
Publicado 2022

A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders

por Suzuki, Toshimitsu, Suzuki, Toshifumi, Raveau, Matthieu, Miyake, Noriko, Sudo, Genki, Tsurusaki, Yoshinori, Watanabe, Takaki, Sugaya, Yuki, Tatsukawa, Tetsuya, Mazaki, Emi, Shimohata, Atsushi, Kushima, Itaru, Aleksic, Branko, Shiino, Tomoko, Toyota, Tomoko, Iwayama, Yoshimi, Nakaoka, Kentaro, Ohmori, Iori, Sasaki, Aya, Watanabe, Ken, Hirose, Shinichi, Kaneko, Sunao, Inoue, Yushi, Yoshikawa, Takeo, Ozaki, Norio, Kano, Masanobu, Shimoji, Takeyoshi, Matsumoto, Naomichi, Yamakawa, Kazuhiro
Publicado 2020