Učitavanje...
Allelic variants of DYX1C1 are not associated with dyslexia in India
Dyslexia is a hereditary neurological disorder that manifests as an unexpected difficulty in learning to read despite adequate intelligence, education, and normal senses. The prevalence of dyslexia ranges from 3 to 15% of the school aged children. Many genetic studies indicated that loci on 6p21.3,...
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| Glavni autori: | , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Medknow Publications
2008
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2840802/ https://ncbi.nlm.nih.gov/pubmed/20300304 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.45002 |
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