The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
Dyslexia is one of the most prevalent childhood cognitive disorders, affecting approximately 5% of school-age children. We have recently identified a risk haplotype associated with dyslexia on chromosome 6p22.2 which spans the TTRAP gene and portions of THEM2 and KIAA0319. Here we show that in the p...
المؤلفون الرئيسيون: | Paracchini, S, Thomas, A, Castro, S, Lai, C, Paramasivam, M, Wang, Y, Keating, B, Taylor, J, Hacking, D, Scerri, T, Francks, C, Richardson, A, Wade-Martins, R, Stein, J, Knight, J, Copp, A, Loturco, J, Monaco, A |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2006
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مواد مشابهة
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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
حسب: Paracchini, S, وآخرون
منشور في: (2006) -
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) -
A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
حسب: Dennis, M, وآخرون
منشور في: (2009) -
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
حسب: Paracchini, S, وآخرون
منشور في: (2008)