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...
المؤلفون الرئيسيون: | 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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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
Public Library of Science
2009
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مواد مشابهة
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A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
حسب: Megan Y Dennis, وآخرون
منشور في: (2009-03-01) -
Expression of the KIAA0319 gene from a haplotype associated with developmental dyslexia
حسب: Dennis, M, وآخرون
منشور في: (2006) -
Further evidence that KIAA0319 is associated with developmental dyslexia
حسب: Harold, D, وآخرون
منشور في: (2006) -
Alternative splicing in the dyslexia-associated gene KIAA0319.
حسب: Velayos-Baeza, A, وآخرون
منشور في: (2007) -
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
حسب: Harold, D, وآخرون
منشور في: (2006)