OXA 1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect
- Submitting institution
-
University of Glasgow
- Unit of assessment
- 5 - Biological Sciences
- Output identifier
- 5-07810
- Type
- D - Journal article
- DOI
-
10.15252/emmm.201809060
- Title of journal
- EMBO Molecular Medicine
- Article number
- e9060
- First page
- -
- Volume
- 10
- Issue
- 11
- ISSN
- 1757-4676
- Open access status
- Compliant
- Month of publication
- November
- Year of publication
- 2018
- URL
-
http://eprints.gla.ac.uk/208996/
- Supplementary information
-
-
- 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
-
24
- Research group(s)
-
-
- Citation count
- -
- Proposed double-weighted
- No
- Reserve for an output with double weighting
- No
- Additional information
- -
- Author contribution statement
- The author made a substantial contribution to the organisation of the conduct of the study AND the author critiqued the output for important intellectual content.
- Non-English
- No
- English abstract
- -
