Wordt geladen...
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...
Bewaard in:
| Gepubliceerd in: | Mol Genet Metab |
|---|---|
| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2014
|
| Onderwerpen: | |
| Online toegang: | 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 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|