Title : Fabry disease - current data and therapeutic approaches.

Pub. Date : 2021 Jan-Mar

PMID : 34609404






1 Functional Relationships(s)
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1 Fabry disease represents an X-linked inherited disorder resulting in the accumulation of globotriaosylceramide (Gb3). globotriaosylceramide alpha 1,4-galactosyltransferase (P blood group) Homo sapiens