Abstract
Intellectual disability is the most common developmental disorder characterized by a congenital limitation in intellectual functioning and adaptive behavior. It often co-occurs with other mental conditions like attention deficit/hyperactivity disorder and autism spectrum disorder, and can be part of a malformation syndrome that affects other organs. Considering the heterogeneity of its causes (environmental and genetic), its frequency worldwide varies greatly. This review focuses on known genes underlying (syndromic and non-syndromic) intellectual disability, it provides a succinct analysis of their Gene Ontology, and it suggests the use of transcriptional profiling for the prioritization of candidate genes.
| Original language | English |
|---|---|
| Pages (from-to) | 599-N/A |
| Number of pages | 16 |
| Journal | F1000Research |
| Volume | 5 |
| DOIs | |
| Publication status | Published - 2016 |
Keywords
- Biochemistry, Genetics and Molecular Biology (all)
- Immunology and Microbiology (all)
- Medicine (all)
- Pharmacology, Toxicology and Pharmaceutics (all)
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