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Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia
Neurodevelopmental disorders that disturb speech and language are highly heritable. Isolation of the underlying genetic risk factors has been hampered by complexity of the phenotype and potentially large number of contributing genes. One exception is the identification of rare heterozygous mutations...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Nature Publishing Group
2009
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2784575/ https://ncbi.nlm.nih.gov/pubmed/19352412 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2009.43 |
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