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Metachromatic Leukodystrophy: Diagnosis, Modeling, and Treatment Approaches
Metachromatic leukodystrophy is a lysosomal storage disease, which is characterized by damage of the myelin sheath that covers most of nerve fibers of the central and peripheral nervous systems. The disease occurs due to a deficiency of the lysosomal enzyme arylsulfatase A (ARSA) or its sphingolipid...
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| Pubblicato in: | Front Med (Lausanne) |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Media S.A.
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7606900/ https://ncbi.nlm.nih.gov/pubmed/33195324 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fmed.2020.576221 |
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