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

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

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

Affiliation

Mueller B; Department of Cell Therapy, Fraunhofer Institute for Cell Therapy and Immunology.

Genes Brain Behav ; 13(3): 350-6, 2014 Mar.

Article in En | MEDLINE | ID: mdl-24373531

Subject(s)

Chromosomes, Human, Pair 18/genetics; Dyslexia/genetics; Polymorphism, Single Nucleotide; Case-Control Studies; Child; Endosomal Sorting Complexes Required for Transport/genetics; Female; Genetic Association Studies; Genetic Predisposition to Disease; Germany; Humans; Male; Myosin Heavy Chains/genetics; Myosin Type V/genetics; Nedd4 Ubiquitin Protein Ligases; Ubiquitin-Protein Ligases/genetics

Key words

Chromosome 18; German primary school students; dyslexia; genetic association studies; genetic predisposition to disease; linkage disequilibrium; quantitative association study; replication study; single nucleotide polymorphism

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 18 / Polymorphism, Single Nucleotide / Dyslexia Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Genes Brain Behav Journal subject: CIENCIAS DO COMPORTAMENTO / GENETICA Year: 2014 Document type: Article Country of publication: United kingdom

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