A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression

Reading disability (RD) or dyslexia is a common neurogenetic disorder. Two genes, KIAA0319 and DCDC2, have been identified by association studies of the DYX2 locus on 6p21.3. We previously identified a 2445 bp deletion, and a compound STR within the deleted region (BV677278), in intron 2 of DCDC2. T...

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Hauptverfasser: Meng, Haiying, Powers, Natalie R., Tang, Ling, Cope, Natalie A., Zhang, Ping-Xia, Fuleihan, Ramsay, Gibson, Christopher, Page, Grier P., Gruen, Jeffrey R.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2010
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3053575/
https://ncbi.nlm.nih.gov/pubmed/21042874
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10519-010-9408-3
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