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Microduplications Disrupting the MYT1L Gene (2p25.3) are Associated with Schizophrenia
Childhood-onset schizophrenia (COS) is a rare severe form of schizophrenia that may have greater salient genetic risk. Despite evidence for high heritability, conclusive genetic causes of schizophrenia remain elusive. Recent genomic technologies in concert with large case-control cohorts, have led t...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3384746/ https://ncbi.nlm.nih.gov/pubmed/22547139 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/YPG.0b013e328353ae3d |
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