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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Bibliografiset tiedot
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2013
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Article
Linkit: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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