文献
J-GLOBAL ID:201602251846382247
整理番号:16A1271598
MIRAGE症候群:SAMD9変異は,新規の全身性疾患であるMIRAGE症候群を引き起こし,7番染色体の欠失に関わる
SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7
著者 (39件):
NARUMI Satoshi
(Keio Univ. School of Medicine, Tokyo, JPN)
,
AMANO Naoko
(Keio Univ. School of Medicine, Tokyo, JPN)
,
ISHII Tomohiro
(Keio Univ. School of Medicine, Tokyo, JPN)
,
HASEGAWA Tomonobu
(Keio Univ. School of Medicine, Tokyo, JPN)
,
KATSUMATA Noriyuki
(National Res. Inst. for Child Health and Dev., Tokyo, JPN)
,
FUKAMI Maki
(National Res. Inst. for Child Health and Dev., Tokyo, JPN)
,
MUROYA Koji
(Kanagawa Children’s Medical Center, Yokohama, JPN)
,
ADACHI Masanori
(Kanagawa Children’s Medical Center, Yokohama, JPN)
,
TOYOSHIMA Katsuaki
(Kanagawa Children’s Medical Center, Yokohama, JPN)
,
TANAKA Yukichi
(Kanagawa Children’s Medical Center, Yokohama, JPN)
,
FUKUZAWA Ryuji
(Tokyo Metropolitan Children’s Medical Center, Tokyo, JPN)
,
MIYAKO Kenichi
(Fukuoka Children’s Hospital, Fukuoka, JPN)
,
KINJO Saori
(Okinawa Prefectural Chubu Hospital, Okinawa, JPN)
,
OHGA Shouichi
(Kyushu Univ., Fukuoka, JPN)
,
IHARA Kenji
(Kyushu Univ., Fukuoka, JPN)
,
INOUE Hirosuke
(Kyushu Univ., Fukuoka, JPN)
,
KINJO Tadamune
(Kyushu Univ., Fukuoka, JPN)
,
HARA Toshiro
(Kyushu Univ., Fukuoka, JPN)
,
KOHNO Miyuki
(Gunma Univ. Graduate School of Medicine, Gunma, JPN)
,
YAMADA Shiro
(Gunma Univ. Graduate School of Medicine, Gunma, JPN)
,
URANO Hironaka
(Gunma Children’s Medical Center, Gunma, JPN)
,
KITAGAWA Yosuke
(Hirosaki Univ. Graduate School of Medicine, Aomori, JPN)
,
TSUGAWA Koji
(Ohdate Municipal Hospital, Ohdate, JPN)
,
HIGA Asumi
(Wakayama Medical Univ., Wakayama, JPN)
,
MIYAWAKI Masakazu
(Wakayama Medical Univ., Wakayama, JPN)
,
OKUTANI Takahiro
(Wakayama Medical Univ., Wakayama, JPN)
,
KIZAKI Zenro
(Japanese Red Cross Kyoto Daiichi Hospital, Kyoto, JPN)
,
HAMADA Hiroyuki
(Japanese Red Cross Kyoto Daiichi Hospital, Kyoto, JPN)
,
KIHARA Minako
(Japanese Red Cross Kyoto Daiichi Hospital, Kyoto, JPN)
,
SHIGA Kentaro
(Yokohama City Univ. Medical Center, Yokohama, JPN)
,
YAMAGUCHI Tetsuya
(Yokohama City Univ. Medical Center, Yokohama, JPN)
,
KENMOCHI Manabu
(Kitasato Univ. School of Medicine, Sagamihara, JPN)
,
KITAJIMA Hiroyuki
(Osaka Medical Center and Res. Inst. for Maternal and Child Health, Osaka, JPN)
,
SHIMIZU Atsushi
(Iwate Medical Univ., Iwate, JPN)
,
KUDOH Jun
(Keio Univ. School of Medicine, Tokyo, JPN)
,
SHIBATA Shinsuke
(Keio Univ. School of Medicine, Tokyo, JPN)
,
OKANO Hideyuki
(Keio Univ. School of Medicine, Tokyo, JPN)
,
MIYAKE Noriko
(Yokohama City Univ. Graduate School of Medicine, Yokohama, JPN)
,
MATSUMOTO Naomichi
(Yokohama City Univ. Graduate School of Medicine, Yokohama, JPN)
資料名:
Nature Genetics
(Nature Genetics)
巻:
48
号:
7
ページ:
792-797
発行年:
2016年07月
JST資料番号:
W0430A
ISSN:
1061-4036
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)