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Article

Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.

Journal of medical genetics - 1 Sept 2004

de Kovel C G F, Hol F A, Heister J G A M, Willemen J J H T, Sandkuijl L A, Franke B, Padberg G W

Abstract excerpt

CONTEXT: Dyslexia is a common disorder with a strong genetic component, but despite significant research effort, the aetiology is still largely unknown. OBJECTIVE: To identify loci contributing to dyslexia risk. METHODS: This was a genomewide linkage analysis in a single large family. Dutch families with at least two first degree relatives suffering from dyslexia participated in the study. Participants were...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 15342694
DOI: 10.1136/jmg.2003.012294
PMCID: PMC1735895

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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