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Development of a model system for neuronal dysfunction in Fabry Disease
Fabry disease is a glycosphingolipid storage disorder that is caused by a genetic deficiency of the enzyme alpha-galactosidase A (AGA, EC 3.2.1.22). It is a multisystem disease that affects the vascular, cardiac, renal, and nervous systems. One of the hallmarks of this disorder is neuropathic pain a...
Tallennettuna:
| Julkaisussa: | Mol Genet Metab |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5031533/ https://ncbi.nlm.nih.gov/pubmed/27471012 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2016.07.010 |
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