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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520281/
https://www.ncbi.nlm.nih.gov/pubmed/32767726
http://dx.doi.org/10.1111/jcmm.15534

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520281/
https://www.ncbi.nlm.nih.gov/pubmed/32767726
http://dx.doi.org/10.1111/jcmm.15534

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