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Identification of candidate intergenic risk loci in autism spectrum disorder
BACKGROUND: Copy number variations (CNVs) and DNA sequence alterations affecting specific neuronal genes are established risk factors for Autism Spectrum Disorder (ASD). In what is largely considered a genetic condition, so far, these mutations account for ~20% of individuals having an ASD diagnosis...
Autores principales: | Walker, Susan, Scherer, Stephen W |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734099/ https://www.ncbi.nlm.nih.gov/pubmed/23879678 http://dx.doi.org/10.1186/1471-2164-14-499 |
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