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A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer
Mutations of FOXP2 in 7q31 cause a rare disorder involving speech apraxia, accompanied by expressive and receptive language impairments. A recent report described a child with speech and language deficits, and a genomic rearrangement affecting chromosomes 7 and 11. One breakpoint mapped to 7q31 and,...
Kaydedildi:
| Yayımlandı: | Mol Cytogenet |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4546047/ https://ncbi.nlm.nih.gov/pubmed/26300977 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-015-0173-0 |
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