文献
J-GLOBAL ID:202102286551817360
整理番号:21A0290170
アジアの小児におけるてんかんにより特徴づけられた13q12.3微小欠失の新規表現型:症例報告【JST・京大機械翻訳】
A novel phenotype of 13q12.3 microdeletion characterized by epilepsy in an Asian child: a case report
著者 (7件):
Wang Mina
(The Department of Acupuncture and Moxibustion, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing Key Laboratory of Acupuncture Neuromodulation, Beijing, China)
,
Wang Mina
(Graduate School, Beijing University of Chinese Medicine, Beijing, China)
,
Li Bin
(The Department of Acupuncture and Moxibustion, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing Key Laboratory of Acupuncture Neuromodulation, Beijing, China)
,
Liao Zehuan
(School of Biological Sciences, Nanyang Technological University, Singapore, Singapore)
,
Liao Zehuan
(Department of Microbiology, Tumor and Cell Biology (MTC), Karolinska Institutet, Biomedicum, Stockholm, Sweden)
,
Jia Yu
(Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China)
,
Fu Yuanbo
(The Department of Acupuncture and Moxibustion, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing Key Laboratory of Acupuncture Neuromodulation, Beijing, China)
資料名:
BMC Medical Genomics (Web)
(BMC Medical Genomics (Web))
巻:
13
号:
1
ページ:
1-6
発行年:
2020年
JST資料番号:
U7308A
ISSN:
1755-8794
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)