De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder

De novo genetic variation is an important class of risk factors for autism spectrum disorder (ASD). Recently, whole exome sequencing of ASD families has identified a novel de novo missense mutation in the human dopamine (DA) transporter (hDAT) gene, which results in a Thr to Met substitution at site...

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Detaylı Bibliyografya
Asıl Yazarlar: Hamilton, Peter J., Campbell, Nicholas G., Sharma, Shruti, Erreger, Kevin, Hansen, Freja Herborg, Saunders, Christine, Belovich, Andrea N., Sahai, Michelle A., Cook, Edwin H., Gether, Ulrik, Mchaourab, Hassane S., Matthies, Heinrich J.G., Sutcliffe, James S., Galli, Aurelio
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2013
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4046646/
https://ncbi.nlm.nih.gov/pubmed/23979605
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2013.102
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