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Vestronidase Alfa: A Review in Mucopolysaccharidosis VII
Mucopolysaccharidosis VII is an extremely rare, autosomal recessive lysosomal storage disorder characterized by a deficiency of β-glucuronidase activity, resulting in partial degradation and accumulation of GAGs in numerous tissues throughout the body, with consequent cellular damage and organ dysfu...
Tallennettuna:
| Julkaisussa: | BioDrugs |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Springer International Publishing
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6469592/ https://ncbi.nlm.nih.gov/pubmed/30848434 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40259-019-00344-7 |
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