Effects of sphingolipids overload on red blood cell properties in Gaucher disease

Gaucher disease (GD) is a genetic disease with mutations in the GBA gene that encodes glucocerebrosidase causing complications such as anaemia and bone disease. GD is characterized by accumulation of the sphingolipids (SL) glucosylceramide (GL1), glucosylsphingosine (Lyso‐GL1), sphingosine (Sph) and...

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Bibliografske podrobnosti
izdano v:J Cell Mol Med
Main Authors: Dupuis, Lucie, Chipeaux, Caroline, Bourdelier, Emmanuelle, Martino, Suella, Reihani, Nelly, Belmatoug, Nadia, Billette de Villemeur, Thierry, Hivert, Bénédicte, Moussa, Fathi, Le Van Kim, Caroline, de Person, Marine, Franco, Mélanie
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2020
Teme:
Original Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7520281/
https://ncbi.nlm.nih.gov/pubmed/32767726
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.15534
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