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Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD
OBJECTIVE: A major motivation for seeking disease-associated genetic variation is to identify novel risk processes. Although rare copy number variants (CNVs) appear to contribute to attention deficit hyperactivity disorder (ADHD), common risk variants (single-nucleotide polymorphisms [SNPs]) have no...
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| Main Authors: | , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Psychiatric Publishing
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3601404/ https://ncbi.nlm.nih.gov/pubmed/22420046 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1176/appi.ajp.2011.11040551 |
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