Altered structural brain connectivity involving the dorsal and ventral language pathways in 16p11.2 deletion syndrome.
Copy number variants at the chromosomal locus 16p11.2 contribute to neurodevelopmental disorders such as autism spectrum disorders, epilepsy, schizophrenia, and language and articulation disorders. Here, we provide detailed findings on the disrupted structural brain connectivity in 16p11.2 deletion...
| Publicado en: | Brain Imaging & Behavior Vol. 13; no. 2; pp. 430 - 446 |
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| Autores principales: | , , , , |
| Formato: | Journal Article |
| Publicado: |
Springer Nature
Apr2019
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| Acceso en línea: | Ver este registro en EBSCOhost |