Title : Human α-Galactosidase A Mutants: Priceless Tools to Develop Novel Therapies for Fabry Disease.

Pub. Date : 2021 Jun 17

PMID : 34204583






1 Functional Relationships(s)
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Protein Name
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1 The absence of the enzyme or its activity results in the accumulation of glycosphingolipids, mainly globotriaosylceramide (Gb3), in different tissues, leading to a wide range of clinical manifestations. globotriaosylceramide alpha 1,4-galactosyltransferase (P blood group) Homo sapiens