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Gaucher disease protects against tuberculosis
Biallelic mutations in the glucocerebrosidase (GBA1) gene cause Gaucher disease, characterized by lysosomal accumulation of glucosylceramide and glucosylsphingosine in macrophages. Gaucher and other lysosomal diseases occur with high frequency in Ashkenazi Jews. It has been proposed that the underly...
Autores principales: | Fan, Jingwen, Hale, Victoria L., Lelieveld, Lindsey T., Whitworth, Laura J., Busch-Nentwich, Elisabeth M., Troll, Mark, Edelstein, Paul H., Cox, Timothy M., Roca, Francisco J., Aerts, Johannes M. F. G., Ramakrishnan, Lalita |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614233/ https://www.ncbi.nlm.nih.gov/pubmed/36745788 http://dx.doi.org/10.1073/pnas.2217673120 |
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