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Tourette syndrome is associated with recurrent exonic copy number variants [Image: see text] [Image: see text]
BACKGROUND: Multiple rare copy number variants (CNVs) including genomic deletions and duplications play a prominent role in neurodevelopmental disorders such as mental retardation, autism, and schizophrenia, but have not been systematically studied in Tourette syndrome (TS). METHODS: We performed a...
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| Hauptverfasser: | , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
American Academy of Neurology
2010
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2876824/ https://ncbi.nlm.nih.gov/pubmed/20427753 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e3181e0f147 |
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