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Cut-like homeobox 1 and nuclear factor I/B mediate ENGRAILED2 autism spectrum disorder-associated haplotype function
Both common and rare variants contribute to autism spectrum disorder (ASD) risk, but few variants have been established as functional. Previously we demonstrated that an intronic haplotype (rs1861972–rs1861973 A–C) in the homeobox transcription factor ENGRAILED2 (EN2) is significantly associated wit...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3298280/ https://ncbi.nlm.nih.gov/pubmed/22180456 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr594 |
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