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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: | , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2013
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| Soggetti: | |
| 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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