Title : Pathogenesis and Molecular Mechanisms of Anderson-Fabry Disease and Possible New Molecular Addressed Therapeutic Strategies.

Pub. Date : 2021 Sep 18

PMID : 34576250






1 Functional Relationships(s)
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1 Lysosomal accumulation of globotriaosylceramide (Gb3) is the element characterizing Fabry disease due to a hereditary deficiency alpha-galactosidase A (GLA) enzyme. globotriaosylceramide alpha 1,4-galactosyltransferase (P blood group) Homo sapiens