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Hemostatic Abnormalities in Gaucher Disease: Mechanisms and Clinical Implications

Gaucher disease (GD) is a rare inherited lysosomal metabolism disorder, characterized by an accumulation into lysosomes of reticuloendothelial cells, especially in the bone marrow, spleen, and liver of β-glucosylceramide and glucosyl sphingosine, which is its deacylated product. Impaired storage is...

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Detalles Bibliográficos
Autores principales: Linari, Silvia, Castaman, Giancarlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9735904/
https://www.ncbi.nlm.nih.gov/pubmed/36498496
http://dx.doi.org/10.3390/jcm11236920

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