文献
J-GLOBAL ID:201802219283937906
整理番号:18A0605810
MSTO1における新たな劣性変異が色素性網膜症のある小脳萎縮を引き起こす
Novel recessive mutations in MSTO1 cause cerebellar atrophy with pigmentary retinopathy
著者 (16件):
IWAMA Kazuhiro
(Yokohama City Univ., Yokohama, JPN)
,
TAKAORI Toru
(National Center of Neurology and Psychiatry, Tokyo, JPN)
,
FUKUSHIMA Ai
(Niigata Prefecture Hamagumi Medical Rehabilitation Center for Disabled Children, Niigata, JPN)
,
TOHYAMA Jun
(Nishi-Niigata Chuo National Hospital, Niigata, JPN)
,
ISHIYAMA Akihiko
(National Center of Neurology and Psychiatry, Tokyo, JPN)
,
OHBA Chihiro
(Yokohama City Univ., Yokohama, JPN)
,
MITSUHASHI Satomi
(Yokohama City Univ., Yokohama, JPN)
,
MIYATAKE Satoko
(Yokohama City Univ., Yokohama, JPN)
,
MIYATAKE Satoko
(Yokohama City Univ. Hospital, Yokohama, JPN)
,
TAKATA Atsushi
(Yokohama City Univ., Yokohama, JPN)
,
MIYAKE Noriko
(Yokohama City Univ., Yokohama, JPN)
,
ITO Shuichi
(Yokohama City Univ., Yokohama, JPN)
,
ITO Shuichi
(Yokohama City Univ. Hospital, Yokohama, JPN)
,
SAITSU Hirotomo
(Hamamatsu Univ. School of Medicine, Hamamatsu, JPN)
,
MIZUGUCHI Takeshi
(Yokohama City Univ., Yokohama, JPN)
,
MATSUMOTO Naomichi
(Yokohama City Univ., Yokohama, JPN)
資料名:
Journal of Human Genetics
(Journal of Human Genetics)
巻:
63
号:
3
ページ:
263-270
発行年:
2018年03月
JST資料番号:
Z0756A
ISSN:
1434-5161
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
イギリス (GBR)
言語:
英語 (EN)