Lucerastat, an iminosugar for substrate reduction therapy in Fabry Disease: Preclinical evidence
Fabry disease (FD) is a lysosomal storage disorder caused by mutations in the GLA gene coding for α-galactosidase A (α-GalA). These mutations lead to the accumulation of α-GalA substrates, including globotriaosylceramide (Gb3). As a consequence of lipid storage, Fabry patients can suffer from neurop...
Những tác giả chính: | Welford, R, Mühleman, A, Priestman, D, Garzotti, M, Deymier, C, Ertel, E, Iglarz, M, Morand, O, Platt, F, Probst, M |
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Định dạng: | Conference item |
Được phát hành: |
Karger
2017
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