Reduced Fronto-Temporal and Limbic Connectivity in the 22q11.2 Deletion Syndrome: Vulnerability Markers for Developing Schizophrenia?

The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of neuroanatomical biomarkers that underlie the risk for developing schizophrenia. Recent advances in magnetic resonance image analyses enable the examination of structural connectivity integrity, scarcel...

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Detalles Bibliográficos
Autores principales: Ottet, Marie-Christine, Schaer, Marie, Cammoun, Leila, Schneider, Maude, Debbané, Martin, Thiran, Jean-Philippe, Eliez, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606218/
https://www.ncbi.nlm.nih.gov/pubmed/23533586
http://dx.doi.org/10.1371/journal.pone.0058429

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606218/
https://www.ncbi.nlm.nih.gov/pubmed/23533586
http://dx.doi.org/10.1371/journal.pone.0058429

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