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Article

Genetic risk variants for dyslexia on chromosome 18 in a German cohort.

Genes, brain, and behavior - 1 Mar 2014

Mueller B, Ahnert P, Burkhardt J, Brauer J, Czepezauer I, Quente E, Boltze J, Wilcke A, Kirsten H

Abstract excerpt

Dyslexia is characterized by impaired reading and spelling. The disorder has a prevalence of about 5% in Germany, and a strong hereditary component. Several loci are thought to be involved in the development of dyslexia. Scerri et al. identified eight potential dyslexia-associated single nucleotide polymorphisms (SNPs) in seven genes on chromosome 18 in an English-speaking population. Here, we present an...

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PMID: 24373531
DOI: 10.1111/gbb.12118

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