Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
University of Zurich · Friedrich-Alexander-Universität Erlangen-Nürnberg · +12 more institutions
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Abstract
No abstract available for this paper.
Citation impact
1,065
total citations
- FWCI
- 60.49
- Percentile
- 100%
- References
- 39
Citations per year
Authors
39- ARAnita Rauch
University of Zurich, Friedrich-Alexander-Universität Erlangen-Nürnberg, Swiss Integrative Center for Human Health
- DWDagmar Wieczorek
Essen University Hospital
- EGElisabeth Graf
Helmholtz Zentrum München
- TWThomas Wieland
Helmholtz Zentrum München
- SESabine Endele
Friedrich-Alexander-Universität Erlangen-Nürnberg
Topics & keywords
Topics
Keywords
- Intellectual disability
- Exome sequencing
- Missense mutation
- Genetics
- Loss function
- Exome
- Indel
- Biology
UN Sustainable Development Goals
- Quality Education
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