Abnormal Auditory Processing and Underlying Structural Changes in 22q11.2 Deletion Syndrome

The 22q11.2 deletion syndrome (22q11.2 DS), one of the highest genetic risk for the development of schizophrenia, offers a unique opportunity to understand neurobiological and functional changes preceding the onset of the psychotic illness. Reduced auditory mismatch negativity response (MMN) has bee...

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Detalles Bibliográficos
Autores principales: Cantonas, Lucia-Manuela, Mancini, Valentina, Rihs, Tonia A, Rochas, Vincent, Schneider, Maude, Eliez, Stephan, Michel, Christoph M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Regular Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7825015/
https://www.ncbi.nlm.nih.gov/pubmed/32747926
http://dx.doi.org/10.1093/schbul/sbaa104

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7825015/
https://www.ncbi.nlm.nih.gov/pubmed/32747926
http://dx.doi.org/10.1093/schbul/sbaa104

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