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 these...

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Publicado en:Brain Struct Funct
Autores principales: 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
Formato: Artigo
Lenguaje:Inglês
Publicado: Springer Berlin Heidelberg 2016
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Original Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5368214/
https://ncbi.nlm.nih.gov/pubmed/27510895
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00429-016-1282-1
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