New Copy Number Variations in Schizophrenia

Genome-wide screenings for copy number variations (CNVs) in patients with schizophrenia have demonstrated the presence of several CNVs that increase the risk of developing the disease and a growing number of large rare CNVs; the contribution of these rare CNVs to schizophrenia remains unknown. Using...

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Detalles Bibliográficos
Autores principales: Magri, Chiara, Sacchetti, Emilio, Traversa, Michele, Valsecchi, Paolo, Gardella, Rita, Bonvicini, Cristian, Minelli, Alessandra, Gennarelli, Massimo, Barlati, Sergio
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954184/
https://www.ncbi.nlm.nih.gov/pubmed/20967226
http://dx.doi.org/10.1371/journal.pone.0013422

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954184/
https://www.ncbi.nlm.nih.gov/pubmed/20967226
http://dx.doi.org/10.1371/journal.pone.0013422

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