Enzyme replacement therapy in type 1 Gaucher disease and a review of the literature
Gaucher disease (GD) is the most common lysosomal storage disorder. Deficiency of the lysosomal enzyme glucocerebrosidase results in the intracellular accumulation of undegraded substrates in the spleen, liver and bone marrow. Enzyme replacement therapy (ERT) is a standard approach for type 1 GD. He...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Turkish Society of Hematology
2010-10-01
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| Serie: | Turkish Journal of Hematology |
| Soggetti: | |
| Accesso online: | https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-73644 |
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