Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability

Reading disability (RD) is a complex genetic disorder with unknown etiology. Genes on chromosome 6p22, including DCDC2, KIAA0319, and TTRAP, have been identified as RD associated genes. Imaging studies have shown both functional and structural differences between brains of individuals with and witho...

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Autori principali: Cope, Natalie, Eicher, John D., Meng, Haiying, Gibson, Christopher J., Hager, Karl, Lacadie, Cheryl, Fulbright, Robert K., Constable, R. Todd, Page, Grier P., Gruen, Jeffrey R.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2012
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3518451/
https://ncbi.nlm.nih.gov/pubmed/22750057
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroimage.2012.06.037
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