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Common genetic variation in the GAD1 gene and the entire family of DLX homeobox genes and autism spectrum disorders
Biological and positional evidence supports the involvement of the GAD1 and distal-less homeobox genes (DLXs) in the etiology of autism. We investigated 42 SNPs in these genes as risk factors for autism spectrum disorders (ASD) in a large family-based association study of 715 nuclear families. No si...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3088769/ https://ncbi.nlm.nih.gov/pubmed/21302352 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.31148 |
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