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Biomarkers in Anderson–Fabry Disease
Fabry disease is a rare lysosomal storage disorder caused by a deficiency of α-galactosidase A, resulting in multisystemic involvement. Lyso-Gb3 (globotriaosylsphingosine), the deacylated form of Gb3, is currently measured in plasma as a biomarker of classic Fabry disease. Intensive research of biom...
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| 發表在: | Int J Mol Sci |
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| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
MDPI
2020
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7662984/ https://ncbi.nlm.nih.gov/pubmed/33138098 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21218080 |
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