Effects of agalsidase-β administration on vascular function and blood pressure in familial Anderson–Fabry disease

Fabry is an X-linked disorder of glycosphingolipid metabolism that is caused by variants of the GLA gene that codes for α-galactosidase A, leading to lysosomal accumulation of globotriaosylceramide in many cell types. As a result, affected patients manifest with an increased risk of developing ische...

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Udgivet i:Eur J Hum Genet
Main Authors: Stamerra, Cosimo Andrea, De Feo, Martina, Castelli, Vanessa, d’Angelo, Michele, Cimini, Annamaria, Grassi, Davide, Ferri, Claudio
Format: Artigo
Sprog:Inglês
Udgivet: Springer International Publishing 2020
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7868353/
https://ncbi.nlm.nih.gov/pubmed/32948848
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-020-00721-9
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