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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Dettagli Bibliografici
Pubblicato in:J Cell Mol Med
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2020
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Original Articles
Accesso online: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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