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Article

Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.

Journal of human genetics - 1 Jul 2015

Matsson Hans, Huss Mikael, Persson Helena, Einarsdottir Elisabet, Tiraboschi Ettore, Nopola-Hemmi Jaana, Schumacher Johannes, Neuhoff Nina, Warnke Andreas, Lyytinen Heikki, Schulte-Körne Gert, Nöthen Markus M, Leppänen Paavo H T, Peyrard-Janvid Myriam, Kere Juha

Abstract excerpt

Genetic studies of complex traits have become increasingly successful as progress is made in next-generation sequencing. We aimed at discovering single nucleotide variation present in known and new candidate genes for developmental dyslexia: CYP19A1, DCDC2, DIP2A, DYX1C1, GCFC2 (also known as C2orf3), KIAA0319, MRPL19, PCNT, PRMT2, ROBO1 and S100B. We used next-generation sequencing to identify single-nucleotide...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Genetic Predisposition to Disease

Share to Microtubule-Associated Proteins

Share to Polymorphism, Single Nucleotide

Share to S100 Calcium Binding Protein beta Subunit

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Source

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Identifiers

PMID: 25877001
DOI: 10.1038/jhg.2015.37
PMCID: PMC4521290

Genes

DCDC2
GCFC2
MRPL19
PCNT
PRMT2
ROBO1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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