Cargando…
Dyslexia risk gene relates to representation of sound in the auditory brainstem
Dyslexia is a reading disorder with strong associations with KIAA0319 and DCDC2. Both genes play a functional role in spike time precision of neurons. Strikingly, poor readers show an imprecise encoding of fast transients of speech in the auditory brainstem. Whether dyslexia risk genes are related t...
Autores principales: | Neef, Nicole E., Müller, Bent, Liebig, Johanna, Schaadt, Gesa, Grigutsch, Maren, Gunter, Thomas C., Wilcke, Arndt, Kirsten, Holger, Skeide, Michael A., Kraft, Indra, Kraus, Nina, Emmrich, Frank, Brauer, Jens, Boltze, Johannes, Friederici, Angela D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987796/ https://www.ncbi.nlm.nih.gov/pubmed/28182973 http://dx.doi.org/10.1016/j.dcn.2017.01.008 |
Ejemplares similares
-
ATP2C2 and DYX1C1 are putative modulators of dyslexia‐related MMR
por: Müller, Bent, et al.
Publicado: (2017) -
Auditory brainstem measures and genotyping boost the prediction of literacy: A longitudinal study on early markers of dyslexia
por: Liebig, Johanna, et al.
Publicado: (2020) -
Dyslexia risk variant rs600753 is linked with dyslexia-specific
differential allelic expression of DYX1C1
por: Müller, Bent, et al.
Publicado: (2018) -
Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort
por: Müller, Bent, et al.
Publicado: (2016) -
Aberrant Prestimulus Oscillations in Developmental Dyslexia Support an Underlying Attention Shifting Deficit
por: Meyer, Lars, et al.
Publicado: (2020)