Llwytho...
Familial manganese-induced neurotoxicity due to mutations in SLC30A10 or SLC39A14
Over the last few years, two rare, familial diseases that lead to the onset of manganese (Mn)-induced neurotoxicity have been discovered. Loss-of-function mutations in SLC30A10, a Mn efflux transporter, or SLC39A14, a Mn influx transporter, increase Mn levels in blood and brain, and induce severe ne...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Neurotoxicology |
|---|---|
| Prif Awdur: | |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2017
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5799044/ https://ncbi.nlm.nih.gov/pubmed/28789954 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuro.2017.07.030 |
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