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A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering
A number of speech disorders including stuttering have been shown to have important genetic contributions, as indicated by high heritability estimates from twin and other studies. We studied the potential contribution to stuttering from variants in the FOXP2 gene, which have previously been associat...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4099264/ https://ncbi.nlm.nih.gov/pubmed/24807205 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2014.04.019 |
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