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...

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Опубликовано в: :Haematologica
Главные авторы: Lefebvre, Thibaud, Reihani, Niloofar, Daher, Raed, de Villemeur, Thierry Billette, Belmatoug, Nadia, Rose, Christian, Colin-Aronovicz, Yves, Puy, Hervé, Le Van Kim, Caroline, Franco, Mélanie, Karim, Zoubida
Формат: Artigo
Язык:Inglês
Опубликовано: Ferrata Storti Foundation 2018
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Article
Online-ссылка: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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