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Glucosylsphingosine but not Saposin C, is the target antigen in Gaucher disease-associated gammopathy
In Gaucher disease type 1 (GD1), genetic deficiency of lysosomal glucocerebrosidase results in the accumulation of glucosylceramide and glucosylsphingosine (GlcSph), that underlie chronic lipid-mediated metabolic inflammation. An important age-related phenotype is high risk of monoclonal gammopathy...
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| 出版年: | Mol Genet Metab |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8223251/ https://ncbi.nlm.nih.gov/pubmed/32044242 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2020.01.009 |
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