A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants
- Submitting institution
-
King's College London
- Unit of assessment
- 4 - Psychology, Psychiatry and Neuroscience
- Output identifier
- 131571760
- Type
- D - Journal article
- DOI
-
10.1038/ejhg.2014.283
- Title of journal
- European Journal of Human Genetics
- Article number
- -
- First page
- 1318
- Volume
- 23
- Issue
- 10
- ISSN
- 1018-4813
- Open access status
- Out of scope for open access requirements
- Month of publication
- February
- Year of publication
- 2015
- URL
-
-
- Supplementary information
-
10.1038/ejhg.2014.283
- 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
-
11
- Research group(s)
-
-
- Citation count
- 50
- Proposed double-weighted
- No
- Reserve for an output with double weighting
- No
- Additional information
- -
- Author contribution statement
- -
- Non-English
- No
- English abstract
- -
