From Cortical and Subcortical Grey Matter Abnormalities to Neurobehavioral Phenotype of Angelman Syndrome: A Voxel-Based Morphometry Study

Angelman syndrome (AS) is a rare neurogenetic disorder due to loss of expression of maternal ubiquitin-protein ligase E3A (UBE3A) gene. It is characterized by severe developmental delay, speech impairment, movement or balance disorder and typical behavioral uniqueness. Affected individuals show norm...

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Detalles Bibliográficos
Autores principales: Aghakhanyan, Gayane, Bonanni, Paolo, Randazzo, Giovanna, Nappi, Sara, Tessarotto, Federica, De Martin, Lara, Frijia, Francesca, De Marchi, Daniele, De Masi, Francesco, Kuppers, Beate, Lombardo, Francesco, Caramella, Davide, Montanaro, Domenico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023118/
https://www.ncbi.nlm.nih.gov/pubmed/27626634
http://dx.doi.org/10.1371/journal.pone.0162817

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023118/
https://www.ncbi.nlm.nih.gov/pubmed/27626634
http://dx.doi.org/10.1371/journal.pone.0162817

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