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A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder
Recent case–control genetic studies of attention deficit hyperactivity disorder (ADHD) have implicated common and rare genetic risk alleles, highlighting the polygenic and complex aetiology of this neurodevelopmental disorder. Studies of other neurodevelopmental disorders, such as autism spectrum di...
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| Vydáno v: | Transl Psychiatry |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group UK
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7217839/ https://ncbi.nlm.nih.gov/pubmed/32398668 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41398-020-0821-y |
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