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Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1
An increasing number of genetic variants involved in dyslexia development were discovered during the last years, yet little is known about the molecular functional mechanisms of these SNPs. In this study we investigated whether dyslexia candidate SNPs have a direct, disease-specific effect on local...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Sociedade Brasileira de Genética
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5901500/ https://www.ncbi.nlm.nih.gov/pubmed/29473935 http://dx.doi.org/10.1590/1678-4685-GMB-2017-0165 |