HIGHLIGHTS
- who: Amaia Carrion-Castillo from the Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands have published the research work: Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family, in the Journal: (JOURNAL) of 19,/02/2016
- what: Until recent years, much of the research on the molecular basis of dyslexia focused on a handful of candidate genes (e_g, ROBO1, KIAA0319, DCDC2, and DYX1C1) that were identified through linkage analysis in families, and then followed up via fine-mapping of association with common variants . . .
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