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Genome-wide analysis identifies a role for common copy number variants in specific language impairment
An exploratory genome-wide copy number variant (CNV) study was performed in 127 independent cases with specific language impairment (SLI), their first-degree relatives (385 individuals) and 269 population controls. Language-impaired cases showed an increased CNV burden in terms of the average number...
Zapisane w:
| Wydane w: | Eur J Hum Genet |
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| Główni autorzy: | , , , , , , , , , , , |
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
Nature Publishing Group
2015
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4592089/ https://ncbi.nlm.nih.gov/pubmed/25585696 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2014.296 |
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