Copy Number Variants in German Patients with Schizophrenia

Large rare copy number variants (CNVs) have been recognized as significant genetic risk factors for the development of schizophrenia (SCZ). However, due to their low frequency (1∶150 to 1∶1000) among patients, large sample sizes are needed to detect an association between specific CNVs and SCZ. So f...

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Detalles Bibliográficos
Autores principales: Priebe, Lutz, Degenhardt, Franziska, Strohmaier, Jana, Breuer, René, Herms, Stefan, Witt, Stephanie H., Hoffmann, Per, Kulbida, Rebecca, Mattheisen, Manuel, Moebus, Susanne, Meyer-Lindenberg, Andreas, Walter, Henrik, Mössner, Rainald, Nenadic, Igor, Sauer, Heinrich, Rujescu, Dan, Maier, Wolfgang, Rietschel, Marcella, Nöthen, Markus M., Cichon, Sven
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/PMC3699619/
https://www.ncbi.nlm.nih.gov/pubmed/23843933
http://dx.doi.org/10.1371/journal.pone.0064035

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699619/
https://www.ncbi.nlm.nih.gov/pubmed/23843933
http://dx.doi.org/10.1371/journal.pone.0064035

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