A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies
- Submitting institution
-
Imperial College of Science, Technology and Medicine
- Unit of assessment
- 1 - Clinical Medicine
- Output identifier
- 3341
- Type
- D - Journal article
- DOI
-
10.1126/scitranslmed.aad7666
- Title of journal
- Science Translational Medicine
- Article number
- ARTN 328ra30
- First page
- -
- Volume
- 8
- Issue
- 328
- ISSN
- 1946-6234
- Open access status
- Out of scope for open access requirements
- Month of publication
- March
- Year of publication
- 2016
- 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
-
42
- Research group(s)
-
B - Cardiovascular
- Citation count
- 52
- 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 conception and design of the study, to the organisation of the conduct of the study and to analysis and interpretation of study data.
The author helped critique the output for important intellectual content.
- Non-English
- No
- English abstract
- -