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The Clinical Management of Type 2 Gaucher Disease
Gaucher disease, the inherited deficiency of the enzyme glucocerebrosidase, is the most common of the lysosomal storage disorders. Type 2 Gaucher disease, the most severe and progressive form, manifests either prenatally or in the first months of life, followed by death within the first years of lif...
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| Опубликовано в: : | Mol Genet Metab |
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| Главные авторы: | , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2014
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4312716/ https://ncbi.nlm.nih.gov/pubmed/25435509 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2014.11.008 |
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