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Structural brain abnormalities in a single gene disorder associated with epilepsy, language impairment and intellectual disability
Childhood speech and language deficits are highly prevalent and are a common feature of neurodevelopmental disorders. However, it is difficult to investigate the underlying causal pathways because many diagnostic groups have a heterogeneous aetiology. Studying disorders with a shared genetic cause a...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2016
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053034/ https://www.ncbi.nlm.nih.gov/pubmed/27747153 http://dx.doi.org/10.1016/j.nicl.2016.07.016 |