Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity

Genome-wide screening for copy number variations (CNVs) in ten Indian dyslexic families revealed the presence of five de novo CNVs in regions harboring GABARAP, NEGR1, ACCN1, DCDC5, and one in already known candidate gene CNTNAP2. These genes are located on regions of chromosomes 17p13.1, 1p31.1, 17...

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Veröffentlicht in:Journal of human genetics 2013-08, Vol.58 (8), p.539-547
Hauptverfasser: Veerappa, Avinash M, Saldanha, Marita, Padakannaya, Prakash, Ramachandra, Nallur B
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Sprache:eng
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