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Published in 2017 at "Molecular genetics and metabolism"
DOI: 10.1016/j.ymgme.2017.06.006
Abstract: BACKGROUND Fabry disease (FD), an X-linked lysosomal storage disorder, results from the deficient activity of α-galactosidase A (α-Gal A) and the accumulation of its substrates, globotriaosylceramide (Gb3) and its deacylated derivative, globotriaosyl-sphingosine (Lyso-Gb3). Here, we…
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Keywords:
gb3 levels;
classic later;
gb3;
lyso gb3 ... See more keywords