Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice

Developmental dyslexia is a common disorder with a strong genetic component, but the underlying molecular mechanisms are still unknown. Several candidate dyslexia-susceptibility genes, including KIAA0319 , DYX1C1, and DCDC2 , have been identified in humans. RNA interference experiments targeting the...

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Veröffentlicht in:Brain Structure and Function 2017-04, Vol.222 (3), p.1367-1384
Hauptverfasser: Martinez-Garay, Isabel, Guidi, Luiz G., Holloway, Zoe G., Bailey, Melissa A. G., Lyngholm, Daniel, Schneider, Tomasz, Donnison, Timothy, Butt, Simon J. B., Monaco, Anthony P., Molnár, Zoltán, Velayos-Baeza, Antonio
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Sprache:eng
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