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Synaptic, transcriptional, and chromatin genes disrupted in autism
The genetic architecture of autism spectrum disorder involves the interplay of common and rare variation and their impact on hundreds of genes. Using exome sequencing, analysis of rare coding variation in 3,871 autism cases and 9,937 ancestry-matched or parental controls implicates 22 autosomal gene...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402723/ https://www.ncbi.nlm.nih.gov/pubmed/25363760 http://dx.doi.org/10.1038/nature13772 |