A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2. Issue 22 (20th November 2021)
- Record Type:
- Journal Article
- Title:
- A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2. Issue 22 (20th November 2021)
- Main Title:
- A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2
- Authors:
- Qiu, Liang-Liang
Lin, Xiao-Dan
Xu, Guo-Rong
Wang, Li-Li
Ye, Zhi-Xian
Lin, Feng
Chen, Hai-Zhu
Lin, Min-Ting
Cai, Nai-Qing
Jin, Ming
Xu, Liu-Qing
Hu, Wei
Wang, Ning
Wang, Zhi-Qiang - Editors:
- Guo, Li-Shao
- Abstract:
- Is Part Of:
- Chinese medical journal. Volume 134:Issue 22(2021)
- Journal:
- Chinese medical journal
- Issue:
- Volume 134:Issue 22(2021)
- Issue Display:
- Volume 134, Issue 22 (2021)
- Year:
- 2021
- Volume:
- 134
- Issue:
- 22
- Issue Sort Value:
- 2021-0134-0022-0000
- Page Start:
- 2753
- Page End:
- 2755
- Publication Date:
- 2021-11-20
- Subjects:
- Medicine -- Periodicals
Medicine, Oriental -- Periodicals
Medicine
Medicine, Oriental
Medicine
Medicine, East Asian Traditional
Periodicals
Electronic journals
610.5 - Journal URLs:
- https://www.ncbi.nlm.nih.gov/pmc/journals/2337/ ↗
https://journals.lww.com/cmj/pages/default.aspx ↗
http://ckrd.cnki.net/grid20/Navi/item.aspx?NaviID=1&BaseID=ZHSS&NaviLink=%e5%8c%bb%e7%96%97%e5%8d%ab%e7%94%9f ↗
http://journals.lww.com/pages/default.aspx ↗ - DOI:
- 10.1097/CM9.0000000000001425 ↗
- Languages:
- English
- ISSNs:
- 0366-6999
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 19880.xml