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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Détails bibliographiques
Auteurs principaux: 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
Format: Artigo
Langue:Inglês
Publié: 2013
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Article
Accès en ligne: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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