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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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| Publicado no: | Schizophr Bull |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7825015/ https://ncbi.nlm.nih.gov/pubmed/32747926 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/schbul/sbaa104 |
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