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Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorder
Autism spectrum disorder (ASD) is a heterogeneous disorder with substantial heritability, most of which is unexplained. ASD has a population prevalence of one percent and affects four times as many males as females. Patients with fragile X E (FRAXE) intellectual disability, which is caused by a sile...
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| Asıl Yazarlar: | , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3441129/ https://ncbi.nlm.nih.gov/pubmed/22773736 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds267 |
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