A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
Numerous genetic association studies have implicated the KIAA0319 gene on human chromosome 6p22 in dyslexia susceptibility. The causative variant(s) remains unknown but may modulate gene expression, given that (1) a dyslexia-associated haplotype has been implicated in the reduced expression of KIAA0...
Asıl Yazarlar: | Dennis, M, Paracchini, S, Scerri, T, Prokunina-Olsson, L, Knight, J, Wade-Martins, R, Coggill, P, Beck, S, Green, E, Monaco, A |
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Materyal Türü: | Journal article |
Dil: | English |
Baskı/Yayın Bilgisi: |
Public Library of Science
2009
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