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High Throughput Screening for Inhibitors of Alpha-Galactosidase
Fabry disease is a rare X-linked lysosomal storage disorder caused by a deficiency in α-galactosidase A (GLA), which catalyzes the hydrolysis of terminal α-galactosyl groups from glycosphingolipids, such as globotriaosylceramide (Gb3). Many of the mutations in the GLA gene are missense alterations t...
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| Huvudupphovsmän: | , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Bentham Open
2010
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3040456/ https://ncbi.nlm.nih.gov/pubmed/21331308 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/1875397301004010067 |
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