Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene. (16th January 2018)
- Record Type:
- Journal Article
- Title:
- Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene. (16th January 2018)
- Main Title:
- Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene
- Authors:
- Yin, Xiao-Meng
Lin, Jing-Han
Cao, Li
Zhang, Tong-Mei
Zeng, Sheng
Zhang, Kai-Lin
Tian, Wo-Tu
Hu, Zheng-Mao
Li, Nan
Wang, Jun-Ling
Guo, Ji-Feng
Wang, Ruo-Xi
Xia, Kun
Zhang, Zhuo-Hua
Yin, Fei
Peng, Jing
Liao, Wei-Ping
Yi, Yong-Hong
Liu, Jing-Yu
Yang, Zhi-Xian
Chen, Zhong
Mao, Xiao
Yan, Xin-Xiang
Jiang, Hong
Shen, Lu
Chen, Sheng-Di
Zhang, Li-Ming
Tang, Bei-Sha - Abstract:
- Is Part Of:
- Human molecular genetics. Volume 27:Number 4(2018:Feb. 15)
- Journal:
- Human molecular genetics
- Issue:
- Volume 27:Number 4(2018:Feb. 15)
- Issue Display:
- Volume 27, Issue 4 (2018)
- Year:
- 2018
- Volume:
- 27
- Issue:
- 4
- Issue Sort Value:
- 2018-0027-0004-0000
- Page Start:
- 757
- Page End:
- 758
- Publication Date:
- 2018-01-16
- Subjects:
- Human molecular genetics -- Periodicals
Human chromosome abnormalities -- Periodicals
572.8 - Journal URLs:
- http://hmg.oxfordjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/hmg/ddy025 ↗
- Languages:
- English
- ISSNs:
- 0964-6906
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4336.198000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14232.xml