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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2013
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3699619/
https://ncbi.nlm.nih.gov/pubmed/23843933
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0064035
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items