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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: Motabar, Omid, Liu, Ke, Southall, Noel, Marugan, Juan J, Goldin, Ehud, Sidransky, Ellen, Zheng, Wei
Médium: Artigo
Jazyk:Inglês
Vydáno: Bentham Open 2010
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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