Učitavanje...
When transporters fail to be transported: how to rescue folding-deficient SLC6 transporters
The human dopamine transporter (hDAT) belongs to the solute carrier 6 (SLC6) gene family. Point mutations in hDAT (SLC6A3) have been linked to a syndrome of dopamine transporter deficiency or infantile dystonia/parkinsonism. The mutations impair DAT folding, causing retention of variant DATs in the...
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| Izdano u: | J Neurol Neuromedicine |
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| Glavni autori: | , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2016
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5386142/ https://ncbi.nlm.nih.gov/pubmed/28405636 |
| Oznake: |
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