Browsing by Author "Maassen, Ben"

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Whole‑genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family

Carrion‑Castillo, Amaia; Estruch, Sara B.; Maassen, Ben; Franke, Barbara; Francks, Clyde; Fisher, Simon E. (Human Genetics, 2021)

Dyslexia is a common heritable developmental disorder involving impaired reading abilities. Its genetic underpinnings are thought to be complex and heterogeneous, involving common and rare genetic variation. Multigenerational ...