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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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Detaylı Bibliyografya
Asıl Yazarlar: Hiroi, Noboru, Hiramoto, Takeshi, Harper, Kathryn M., Suzuki, Go, Boku, Shuken
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2012
Konular:
Online Erişim: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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