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Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model
Although twin studies indicate clear genetic bases of autism spectrum disorder (ASD), the precise mechanisms through which genetic variations causally result in ASD are poorly understood. Individuals with 3 Mb and nested 1.5 Mb hemizygosity of the chromosome 22q11.2 represent genetically identifiabl...
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| Autores principales: | , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Oxford University Press
2011
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3221538/ https://ncbi.nlm.nih.gov/pubmed/21908517 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr404 |
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