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Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome
OBJECTIVE: 22q11.2 deletion syndrome (22q11.2DS) is associated with a >20-fold increased risk for developing schizophrenia. The aim of this study was to identify additional genetic factors (i.e., “second hits”) that may contribute to schizophrenia expression. METHODS: Through an international con...
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| Publié dans: | Am J Psychiatry |
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| Auteurs principaux: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2017
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5665703/ https://ncbi.nlm.nih.gov/pubmed/28750581 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1176/appi.ajp.2017.16121417 |
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