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Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample
Authors:Kerstin U. Ludwig  Darina Roeske  Johannes Schumacher  Gerd Schulte-Körne  Inke R. König  Andreas Warnke  Ellen Plume  Andreas Ziegler  Helmut Remschmidt  Bertram Müller-Myhsok  Markus M. Nöthen  Per Hoffmann
Affiliation:Department of Genomics, Life and Brain Center, University of Bonn, Sigmund-Freud Str. 25, 53105, Bonn, Germany.
Abstract:The dyslexia susceptibility locus DYX2 (chr. 6p21-p22) harbours two candidate genes, DCDC2 and KIAA0319. In 2006, Harold et al. reported evidence for interaction between both genes. Having previously identified a risk haplotype for dyslexia in DCDC2, but not KIAA0319, in German families, we also tested for interaction between this risk haplotype and KIAA0319. We found a nominally significant association for the quantitative dimension “word reading”, the core phenotype in the study of Harold et al., which may be considered as supportive evidence.
Keywords:DYX2  Doublecortin domain  Interaction  Reading  Spelling
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