Embryonic disruption of the candidate dyslexia susceptibility gene homologue Kiaa0319-like results in neuronal migration disorders

Developmental dyslexia, the most common childhood learning disorder, is highly heritable, and recent studies have identified KIAA0319-Like (KIAA0319L) as a candidate dyslexia susceptibility gene at the 1p36-34 (DYX8) locus. In this experiment, we investigated the anatomical effects of knocking down...

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Autori principali: Platt, MP, Adler, WT, Mehlhorn, AJ, Johnson, GC, Wright, KA, Choi, RT, Tsang, WH, Poon, MW, Yeung, SY, Waye, MMY, Galaburda, AM, Rosen, GD
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2013
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3843998/
https://ncbi.nlm.nih.gov/pubmed/23831424
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2013.06.056
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