文献
J-GLOBAL ID:201702221815240872
整理番号:17A1162018
ポリコーム抑制複合体2サブユニットをコードする遺伝子における変異は,Weaver症候群を引き起こす【Powered by NICT】
Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome
著者 (19件):
Imagawa Eri
(Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan)
,
Higashimoto Ken
(Division of Molecular Genetics and Epigenetics, Department of Biomolecular Sciences, Faculty of Medicine, Saga University, Saga, Japan)
,
Sakai Yasunari
(Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan)
,
Numakura Chikahiko
(Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan)
,
Okamoto Nobuhiko
(Department of Medical Genetics, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan)
,
Matsunaga Satoko
(Department of Microbiology, Yokohama City University School of Medicine, Yokohama, Japan)
,
Ryo Akihide
(Department of Microbiology, Yokohama City University School of Medicine, Yokohama, Japan)
,
Sato Yoshinori
(Department of Molecular Biology, Yokohama City University School of Medicine, Yokohama, Japan)
,
Sanefuji Masafumi
(Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan)
,
Ihara Kenji
(Department of Pediatrics, Faculty of Medicine, Oita University, Yufu, Japan)
,
Takada Yui
(Department of Pediatrics, Japanese Red Cross Fukuoka Hospital, Fukuoka, Japan)
,
Nishimura Gen
(Department of Pediatric Imaging, Tokyo Metropolitan Children’s Medical Center, Tokyo, Japan)
,
Saitsu Hirotomo
(Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan)
,
Mizuguchi Takeshi
(Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan)
,
Miyatake Satoko
(Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan)
,
Nakashima Mitsuko
(Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan)
,
Miyake Noriko
(Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan)
,
Soejima Hidenobu
(Division of Molecular Genetics and Epigenetics, Department of Biomolecular Sciences, Faculty of Medicine, Saga University, Saga, Japan)
,
Matsumoto Naomichi
(Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan)
資料名:
Human Mutation
(Human Mutation)
巻:
38
号:
6
ページ:
637-648
発行年:
2017年
JST資料番号:
W2601A
ISSN:
1059-7794
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
アメリカ合衆国 (USA)
言語:
英語 (EN)