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Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders
Recently discovered genome-wide rare copy number variants (CNVs) have unprecedented levels of statistical association with many developmental neuropsychiatric disorders, including schizophrenia, autism spectrum disorders, intellectual disability and attention deficit hyperactivity disorder. However,...
Gorde:
| Egile Nagusiak: | , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2013
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3852900/ https://ncbi.nlm.nih.gov/pubmed/23917946 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2013.92 |
| Etiketak: |
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