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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2022
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| 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 |