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SLC30A10: A novel manganese transporter
Homozygous mutations in SLC30A10 cause familial parkinsonism associated with manganese (Mn) retention. We recently identified SLC30A10 to be a cell surface-localized Mn efflux transporter and demonstrated that parkinsonism-causing mutations block its intracellular trafficking and efflux function. In...
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| Publicado no: | Worm |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4588552/ https://ncbi.nlm.nih.gov/pubmed/26430566 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/21624054.2015.1042648 |
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