Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome

The 22q11.2 Deletion Syndrome (22q11.2 DS) is one of the highest genetic risk factors for the development of schizophrenia spectrum disorders. In schizophrenia, reduced amplitude of the frequency mismatch negativity (fMMN) has been proposed as a promising neurophysiological marker for progressive br...

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Detalles Bibliográficos
Autores principales: Cantonas, Lucia-Manuela, Tomescu, Miralena I., Biria, Marjan, Jan, Reem K., Schneider, Maude, Eliez, Stephan, Rihs, Tonia A., Michel, Christoph M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467880/
https://www.ncbi.nlm.nih.gov/pubmed/30992427
http://dx.doi.org/10.1038/s41398-019-0473-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467880/
https://www.ncbi.nlm.nih.gov/pubmed/30992427
http://dx.doi.org/10.1038/s41398-019-0473-y

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