ACTB loss-of-function mutations result in a pleiotropic developmental disorder
- Submitting institution
-
The University of Manchester
- Unit of assessment
- 1 - Clinical Medicine
- Output identifier
- 64800873
- Type
- D - Journal article
- DOI
-
10.1016/j.ajhg.2017.11.006
- Title of journal
- American Journal of Human Genetics
- Article number
- -
- First page
- 1021
- Volume
- 101
- Issue
- 6
- ISSN
- 0002-9297
- Open access status
- Compliant
- Month of publication
- December
- Year of publication
- 2017
- URL
-
-
- 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
- No
- Number of additional authors
-
40
- Research group(s)
-
I - Cell Matrix Biology and Regenerative Medicine
- Citation count
- 35
- Proposed double-weighted
- No
- Reserve for an output with double weighting
- No
- Additional information
- -
- Author contribution statement
- I was involved in data acquisition and analysis from mouse tissues, and was involved in providing and critiquing the intellectual content to the publication.
- Non-English
- No
- English abstract
- -
