Rare mosaic variant of GJA1 in a patient with a neurodevelopmental disorder by Rina Shimomura, Tomoe Yanagishita, Kumiko Ishiguro, Minobu Shichiji, Takatoshi Sato, Keiko Shimojima Yamamoto, Miho Nagata, Yasuki Ishihara, Yohei Miyashita, Keiko Ishigaki, Satoru Nagata, Yoshihiro Asano, Toshiyuki Yamamoto

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Characteristic craniofacial defects associated with a novel USP9X truncation mutation by Namiki Nagata, Hiroshi Kurosaka, Kotaro Higashi, Masaya Yamaguchi, Sayuri Yamamoto, Toshihiro Inubushi, Miho Nagata, Yasuki Ishihara, Ayumi Yonei, Yohei Miyashita, Yoshihiro Asano, Norio Sakai, Yasushi Sakata, Shigetada Kawabata, Takashi Yamashiro

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Four cardiomyopathy patients with a heterozygous DSG2 p.Arg119Ter variant by Takuya Sumida, Shou Ogawa, Shuichiro Higo, Yuki Kuramoto, Ryo Eto, Yoshihiko Ikeda, Congcong Sun, Junjun Li, Li Liu, Tomoka Tabata, Yoshihiro Asano, Mikio Shiba, Yasuhiro Akazawa, Daisuke Nakamura, Takafumi Oka, Tomohito Ohtani, Yasushi Sakata

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Sarcomere gene variants did not improve cardiac function in pediatric patients with dilated cardiomyopathy from Japanese cohorts by Keiichi Hirono, Yukiko Hata, Shojiro Ichimata, Naoki Nishida, Teruhiko Imamura, Yoshihiro Asano, Yuki Kuramoto, Kaori Tsuboi, Shinya Takarada, Mako Okabe, Hideyuki Nakaoka, Keijiro Ibuki, Sayaka Ozawa, Jun Muneuchi, Kazushi Yasuda, Kotaro Urayama, Hideharu Oka, Tomoyuki Miyamoto, Kenji Baba, Akio Kato, Hirofumi Saiki, Naoki Kuwabara, Masako Harada, Shiro Baba, Mari Morikawa, Hidenori Iwasaki, Yuichiro Hirata, Yuki Ito, Heima Sakaguchi, Susumu Urata, Koichi Toda, Emi Kittaka, Seigo Okada, Yohei Hasebe, Shinsuke Hoshino, Takanari Fujii, Norie Mitsushita, Masaki Nii, Kayo Ogino, Mitsuhiro Fujino, Yoko Yoshida, Yutaka Fukuda, Satoru Iwashima, Kiyohiro Takigiku, Yasushi Sakata, Ryo Inuzuka, Jun Maeda, Yasunobu Hayabuchi, Tao Fujioka, Hidemasa Namiki, Shuhei Fujita, Koichi Nishida, Ayako Kuraoka, Nobuhiko Kan, Sachiko Kido, Ken Watanabe, Fukiko Ichida

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