Germline Mutations in SUFU Cause Gorlin Syndrome–Associated Childhood Medulloblastoma and Redefine the Risk Associated With PTCH1 Mutations
- Submitting institution
-
The University of Manchester
- Unit of assessment
- 2 - Public Health, Health Services and Primary Care
- Output identifier
- 155414156
- Type
- D - Journal article
- DOI
-
10.1200/JCO.2014.58.2569
- Title of journal
- Journal of Clinical Oncology
- Article number
- -
- First page
- 4155
- Volume
- 32
- Issue
- 36
- ISSN
- 0732-183X
- Open access status
- Out of scope for open access requirements
- Month of publication
- November
- Year of publication
- 2014
- 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
- Yes
- Number of additional authors
-
14
- Research group(s)
-
G - Cancer Sciences
- Citation count
- 127
- Proposed double-weighted
- No
- Reserve for an output with double weighting
- No
- Additional information
- -
- Author contribution statement
- -
- Non-English
- No
- English abstract
- -
