A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome
- Submitting institution
-
University of Exeter
- Unit of assessment
- 1 - Clinical Medicine
- Output identifier
- 75
- Type
- D - Journal article
- DOI
-
10.1038/ng.3313
- Title of journal
- Nature Genetics
- Article number
- -
- First page
- 814
- Volume
- 47
- Issue
- 7
- ISSN
- 1061-4036
- Open access status
- Out of scope for open access requirements
- Month of publication
- May
- Year of publication
- 2015
- URL
-
-
- Supplementary information
-
https://www.nature.com/articles/ng.3313#Sec12
- 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
-
15
- Research group(s)
-
B - Neuroscience and Mental Health
- Citation count
- 63
- 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 analysis and interpretation of study data and the author helped draft the output.
- Non-English
- No
- English abstract
- -