Patient centered guidelines for the laboratory diagnosis of Gaucher disease type 1

Gaucher disease (GD) is an autosomal recessive lysosomal storage disorder due to the deficient activity of the acid beta-glucosidase (GCase) enzyme, resulting in the progressive lysosomal accumulation of glucosylceramide (GlcCer) and its deacylated derivate, glucosylsphingosine (GlcSph). GCase is en...

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Detalles Bibliográficos
Autores principales: Dardis, A., Michelakakis, H., Rozenfeld, P., Fumic, K., Wagner, J., Pavan, E., Fuller, M., Revel-Vilk, S., Hughes, D., Cox, T., Aerts, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768924/
https://www.ncbi.nlm.nih.gov/pubmed/36544230
http://dx.doi.org/10.1186/s13023-022-02573-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768924/
https://www.ncbi.nlm.nih.gov/pubmed/36544230
http://dx.doi.org/10.1186/s13023-022-02573-6

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