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Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
Rare copy number variants (CNVs) disrupting ASTN2 or both ASTN2 and TRIM32 have been reported at 9q33.1 by genome-wide studies in a few individuals with neurodevelopmental disorders (NDDs). The vertebrate-specific astrotactins, ASTN2 and its paralog ASTN1, have key roles in glial-guided neuronal mig...
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Päätekijät: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Aineistotyyppi: | Artigo |
Kieli: | Inglês |
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Oxford University Press
2014
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Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3990173/ https://ncbi.nlm.nih.gov/pubmed/24381304 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt669 |
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