Altered Development of the Dorsolateral Prefrontal Cortex in Chromosome 22q11.2 Deletion Syndrome: an in vivo (1)H Spectroscopy study

BACKGROUND: Chromosome 22q11.2 deletion syndrome (22q11DS), the most common microdeletion in humans, is associated with multiple medical features, almost universal cognitive deficits, and a high-risk of schizophrenia. The metabolic basis of the psychological/psychiatric features is not well understo...

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Detalhes bibliográficos
Main Authors: Shashi, Vandana, Veerapandiyan, Aravindhan, Keshavan, Matcheri S., Zapadka, Michael, Schoch, Kelly, Kwapil, Thomas R., Hooper, Stephen R., Stanley, Jeffrey A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3440535/
https://ncbi.nlm.nih.gov/pubmed/22633947
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biopsych.2012.04.023
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