Heimler Syndrome is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6
- Submitting institution
-
The University of Leeds
- Unit of assessment
- 3 - Allied Health Professions, Dentistry, Nursing and Pharmacy
- Output identifier
- UOA3-1002
- Type
- D - Journal article
- DOI
-
10.1016/j.ajhg.2015.08.011
- Title of journal
- American Journal of Human Genetics
- Article number
- -
- First page
- 535
- Volume
- 97
- Issue
- 4
- ISSN
- 0002-9297
- Open access status
- Out of scope for open access requirements
- Month of publication
- September
- Year of publication
- 2015
- URL
-
-
- Supplementary information
-
http://dx.doi.org/10.1016/j.ajhg.2015.08.011
- 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
-
30
- Research group(s)
-
B - Dentistry
- Citation count
- 53
- Proposed double-weighted
- No
- Reserve for an output with double weighting
- No
- Additional information
- -
- Author contribution statement
- Contribution A: Contribution to the conception and design of the study
Contribution B: Critique the output for important intellectual content
- Non-English
- No
- English abstract
- -