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Involvement of hepcidin in iron metabolism dysregulation in Gaucher disease
Gaucher disease (GD) is an inherited deficiency of glucocerebrosidase leading to accumulation of glucosylceramide in tissues such as the spleen, liver, and bone marrow. The resulting lipid-laden macrophages lead to the appearance of “Gaucher cells”. Anemia associated with an unexplained hyperferriti...
Gorde:
| Argitaratua izan da: | Haematologica |
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| Egile Nagusiak: | , , , , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Ferrata Storti Foundation
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5865418/ https://ncbi.nlm.nih.gov/pubmed/29305416 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2017.177816 |
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