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 |
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