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A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression
Reading disability (RD) or dyslexia is a common neurogenetic disorder. Two genes, KIAA0319 and DCDC2, have been identified by association studies of the DYX2 locus on 6p21.3. We previously identified a 2445 bp deletion, and a compound STR within the deleted region (BV677278), in intron 2 of DCDC2. T...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3053575/ https://ncbi.nlm.nih.gov/pubmed/21042874 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10519-010-9408-3 |
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