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Zn(2+) reverses functional deficits in a de novo dopamine transporter variant associated with autism spectrum disorder
Our laboratory recently characterized a novel autism spectrum disorder (ASD)-associated de novo missense mutation in the human dopamine transporter (hDAT) gene SLC6A3 (hDAT T356M). This hDAT variant exhibits dysfunctional forward and reverse transport properties that may contribute to DA dysfunction...
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| Pubblicato in: | Mol Autism |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4349303/ https://ncbi.nlm.nih.gov/pubmed/25741436 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13229-015-0002-7 |
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