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Copy number variation and brain structure: lessons learned from chromosome 16p11.2
Recent work has linked specific genetic variation found in human populations to risk for developing neuropsychiatric diseases. How that risk is mediated through molecular-, cellular- and systems-level mechanisms now becomes the central question in this field. Two recent papers studying high-penetran...
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| Publié dans: | Genome Med |
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| Auteur principal: | |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2015
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4329653/ https://ncbi.nlm.nih.gov/pubmed/25688292 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-015-0140-8 |
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