Assessment of Gene Variant Amenability for Pharmacological Chaperone Therapy with 1-Deoxygalactonojirimycin in Fabry Disease

Fabry disease is one of the most common lysosomal storage disorders caused by mutations in the gene encoding lysosomal α-galactosidase A (α-Gal A) and resultant accumulation of glycosphingolipids. The sugar mimetic 1-deoxygalactonojirimycin (DGJ), an orally available pharmacological chaperone, was c...

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Detalles Bibliográficos
Autores principales: Lukas, Jan, Cimmaruta, Chiara, Liguori, Ludovica, Pantoom, Supansa, Iwanov, Katharina, Petters, Janine, Hund, Christina, Bunschkowski, Maik, Hermann, Andreas, Cubellis, Maria Vittoria, Rolfs, Arndt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037350/
https://www.ncbi.nlm.nih.gov/pubmed/32023956
http://dx.doi.org/10.3390/ijms21030956

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037350/
https://www.ncbi.nlm.nih.gov/pubmed/32023956
http://dx.doi.org/10.3390/ijms21030956

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