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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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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Bentham Open
2010
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| Témata: | |
| On-line přístup: | 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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