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...

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Detalles Bibliográficos
Autores principales: Müller, Bent, Boltze, Johannes, Czepezauer, Ivonne, Hesse, Volker, Wilcke, Arndt, Kirsten, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Genética 2018
Materias:
Human and Medical Genetics
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

Internet

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

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