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Article

Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Oct 2014

Veerappa Avinash M, Saldanha Marita, Padakannaya Prakash, Ramachandra Nallur B

Abstract excerpt

Developmental dyslexia (DD) is a complex heritable disorder with unexpected difficulty in learning to read and spell despite adequate intelligence, education, environment, and normal senses. We performed genome-wide screening for copy number variations (CNVs) in 10 large Indian dyslexic families using Affymetrix Genome-Wide Human SNP Array 6.0. Results revealed the complex genomic rearrangements due to one...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 25139666
DOI: 10.1002/ajmg.b.32260

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NSF

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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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