The dopamine transporter gene SLC6A3: multidisease risks

The human dopamine transporter gene SLC6A3 has been consistently implicated in several neuropsychiatric diseases but the disease mechanism remains elusive. In this risk synthesis, we have concluded that SLC6A3 represents an increasingly recognized risk with a growing number of familial mutants assoc...

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Detalles Bibliográficos
Autores principales: Reith, Maarten E. A., Kortagere, Sandhya, Wiers, Corinde E., Sun, Hui, Kurian, Manju A., Galli, Aurelio, Volkow, Nora D., Lin, Zhicheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9008071/
https://www.ncbi.nlm.nih.gov/pubmed/34650206
http://dx.doi.org/10.1038/s41380-021-01341-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9008071/
https://www.ncbi.nlm.nih.gov/pubmed/34650206
http://dx.doi.org/10.1038/s41380-021-01341-5

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