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Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

Abstract:

Dyslexia is one of the most common childhood disorders with a prevalence of around 5-10% in school-age children. Although an important genetic component is known to have a role in the aetiology of dyslexia, we are far from understanding the molecular mechanisms leading to the disorder. Several candidate genes have been implicated in dyslexia, including DYX1C1, DCDC2, KIAA0319, and the MRPL19/C2ORF3 locus, each with reports of both positive and no replications. We generated a European cross-li...

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Publisher copy:
10.1038/ejhg.2013.199

Authors


Czamara, D More by this author
Scerri, TS More by this author
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Publisher:
Nature Publishing Group
Journal:
European Journal of Human Genetics
Volume:
22
Issue:
5
Pages:
675-680
Publication date:
2014
DOI:
EISSN:
1476-5438
ISSN:
1018-4813
URN:
uuid:5a9dd76a-87f0-4e7c-b3c4-7520ea3bc475
Source identifiers:
464180
Local pid:
pubs:464180

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