Yüklüyor......
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...
Kaydedildi:
| Asıl Yazarlar: | , , , , , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2011
|
| Konular: | |
| Online Erişim: | 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 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|