文献
J-GLOBAL ID:201702256548052992
整理番号:17A1827922
構成的小胞体ストレスに至るWFS1遺伝子の新規ヘテロ接合性突然変異はWolfram症候群の原因である【Powered by NICT】
A novel heterozygous mutation of the WFS1 gene leading to constitutive endoplasmic reticulum stress is the cause of Wolfram syndrome
著者 (7件):
Morikawa Shuntaro
(Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan)
,
Tajima Toshihiro
(Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan)
,
Tajima Toshihiro
(Department of Pediatrics, Jichi Children’s Medical Center, Shimotsuke, Japan)
,
Nakamura Akie
(Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan)
,
Nakamura Akie
(Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan)
,
Ishizu Katsura
(Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan)
,
Ariga Tadashi
(Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan)
資料名:
Pediatric Diabetes
(Pediatric Diabetes)
巻:
18
号:
8
ページ:
934-941
発行年:
2017年
JST資料番号:
W2717A
ISSN:
1399-543X
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)