文献
J-GLOBAL ID:201602277828259855
整理番号:16A0329379
Kindler症候群の中国人患者におけるFERMT1遺伝子の新規大型欠失突然変異【Powered by NICT】
A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome
著者 (9件):
Gao Ying
(Capital Inst. of Pediatrics, Beijing)
,
Bai Jinli
(Capital Inst. of Pediatrics, Beijing)
,
Liu Xiaoyan
(Capital Inst. of Pediatrics, Beijing)
,
Qu Yujin
(Capital Inst. of Pediatrics, Beijing)
,
Cao Yanyan
(Capital Inst. of Pediatrics, Beijing)
,
Wang Jiancai
(Capital Inst. of Pediatrics, Beijing)
,
Jin Yuwei
(Capital Inst. of Pediatrics, Beijing)
,
Wang Hong
(Capital Inst. of Pediatrics, Beijing)
,
Song Fang
(Capital Inst. of Pediatrics, Beijing)
資料名:
Journal of Zhejiang University - Science B. Biomedicine & Biotechnology
(Journal of Zhejiang University - Science B. Biomedicine & Biotechnology)
巻:
16
号:
11
ページ:
957-962
発行年:
2015年
JST資料番号:
W1572A
ISSN:
1673-1581
CODEN:
JZUSAM
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
中国 (CHN)
言語:
英語 (EN)