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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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| Hlavní autoři: | , , , , , , , , , , , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2013
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| Témata: | |
| On-line přístup: | 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 |
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