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Strong Motion Deficits in Dyslexia Associated with DCDC2 Gene Alteration
Dyslexia is a specific impairment in reading that affects 1 in 10 people. Previous studies have failed to isolate a single cause of the disorder, but several candidate genes have been reported. We measured motion perception in two groups of dyslexics, with and without a deletion within the DCDC2 gen...
Uloženo v:
| Vydáno v: | J Neurosci |
|---|---|
| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Society for Neuroscience
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4888943/ https://ncbi.nlm.nih.gov/pubmed/26019324 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.5077-14.2015 |
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