Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
- Submitting institution
-
University of Nottingham, The
- Unit of assessment
- 1 - Clinical Medicine
- Output identifier
- 1333817
- Type
- D - Journal article
- DOI
-
10.1002/ajmg.a.36887
- Title of journal
- American Journal of Medical Genetics Part A
- Article number
- -
- First page
- 296
- Volume
- 167
- Issue
- 2
- ISSN
- 1552-4825
- Open access status
- Out of scope for open access requirements
- Month of publication
- January
- Year of publication
- 2015
- 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
-
135
- Research group(s)
-
A - Child Health, Obstetrics and Gynaecology
- Citation count
- 237
- Proposed double-weighted
- No
- Reserve for an output with double weighting
- No
- Additional information
- -
- Author contribution statement
- The author made a substantial contribution to carrying out the study
The author helped critique the output for important intellectual content
The author helped draft the output
- Non-English
- No
- English abstract
- -
