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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Detalhes bibliográficos
Publicado no: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
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
Assuntos:
Original Articles
Acesso em linha: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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