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Determination of globotriaosylceramide analogs in the organs of a mouse model of Fabry disease
Fabry disease is a heritable lipid disorder caused by the low activity of α-galactosidase A and characterized by the systemic accumulation of globotriaosylceramide (Gb3). Recent studies have reported a structural heterogeneity of Gb3 in Fabry disease, including Gb3 isoforms with different fatty acid...
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| Published in: | J Biol Chem |
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| Main Authors: | , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
American Society for Biochemistry and Molecular Biology
2020
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7186183/ https://ncbi.nlm.nih.gov/pubmed/32179651 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.RA120.012665 |
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