Intellectual Disability and Blended Phenotypes: Insights from a Centre in North India
Intellectual disability (ID) is seen in around 2.5% of global population and can vary from mild to severe and profound ID. There can be multiple affected family members if it is inherited, though many autosomal dominant ID cases would be due to de novo mutations are very less likely to recur in fami...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Wiley
2024-01-01
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| Col·lecció: | Case Reports in Genetics |
| Accés en línia: | http://dx.doi.org/10.1155/2024/6009569 |
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