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An investigation of NFXL1, a gene implicated in a study of specific language impairment
BACKGROUND: A recent study identified NFXL1 as a candidate gene for specific language impairment. The protein encoded by this gene is predicted to be a transcription factor based on domain similarities with NFX1, a repressor of HLA class II genes, which have themselves been implicated in specific la...
Kaydedildi:
| Yayımlandı: | J Neurodev Disord |
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| Yazar: | |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4822306/ https://ncbi.nlm.nih.gov/pubmed/27053962 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-016-9146-9 |
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