Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization
- Submitting institution
-
University of Exeter
- Unit of assessment
- 1 - Clinical Medicine
- Output identifier
- 137
- Type
- D - Journal article
- DOI
-
10.1093/brain/awx249
- Title of journal
- Brain
- Article number
- -
- First page
- 2838
- Volume
- 140
- Issue
- 11
- ISSN
- 0006-8950
- Open access status
- Not compliant
- Month of publication
- October
- Year of publication
- 2017
- URL
-
-
- Supplementary information
-
https://academic.oup.com/brain/article/140/11/2838/4568330#supplementary-data
- Request cross-referral to
- -
- Output has been delayed by COVID-19
- No
- COVID-19 affected output statement
- -
- Forensic science
- No
- Criminology
- No
- Interdisciplinary
- Yes
- Number of additional authors
-
23
- Research group(s)
-
B - Neuroscience and Mental Health
- Citation count
- 12
- Proposed double-weighted
- No
- Reserve for an output with double weighting
- No
- Additional information
- -
- Author contribution statement
- -
- Non-English
- No
- English abstract
- -