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Mouse Models of 22q11.2-Associated Autism Spectrum Disorder
Copy number variation (CNV) of human chromosome 22q11.2 is associated with an elevated rate of autism spectrum disorder (ASD) and represents one of syndromic ASDs with rare genetic variants. However, the precise genetic basis of this association remains unclear due to its relatively large hemizygous...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4118685/ https://ncbi.nlm.nih.gov/pubmed/25089229 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4172/2165-7890.S1-001 |
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