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Fabry disease and incidence of cancer

Abstract Background Fabry disease is an X-linked lysosomal storage disorder caused by deficient activity of α-galactosidase A and the resulting accumulation of the glycosphingolipid globotriaosylceramide (Gb3) and its derivatives, including globotriaosylsphingosine (Lyso-Gb3). Increased cellular and...

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Bibliografiske detaljer
Principais autores: Sarah Bird, Efthymios Hadjimichael, Atul Mehta, Uma Ramaswami, Derralynn Hughes
Format: Artigo
Sprog:Inglês
Udgivet: BMC 2017-09-01
Serier:Orphanet Journal of Rare Diseases
Fag:
Online adgang:http://link.springer.com/article/10.1186/s13023-017-0701-6
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