Common variation within the SETBP1 gene is associated with reading-related skills and patterns of functional neural activation

Volume: 130, Pages: 44 - 51
Published: Jul 1, 2019
Abstract
Epidemiological population studies highlight the presence of substantial individual variability in reading skill, with approximately 5–10% of individuals characterized as having specific reading disability (SRD). Despite reported substantial heritability, typical for a complex trait, the specifics of the connections between reading and the genome are not understood. Recently, the SETBP1 gene has been implicated in several complex...
Paper Details
Title
Common variation within the SETBP1 gene is associated with reading-related skills and patterns of functional neural activation
Published Date
Jul 1, 2019
Volume
130
Pages
44 - 51
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