Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia
Copy number variations (CNVs) account for a substantial proportion of human genomic variation, and have been shown to cause neurodevelopmental disorders.We sought to determine the relevance of CNVs to the aetiology of schizophrenia (SZ).Whole-genome, high-resolution, tiling path BAC array comparativ...
Gardado en:
| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | inglés |
| Publicado: |
2007
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| Acceso en liña: | https://doi.org/10.1093/hmg/ddm323 |
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