Title : DNA methylation impact on Fabry disease.

Pub. Date : 2021 Feb 2

PMID : 33531072






1 Functional Relationships(s)
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1 BACKGROUND: Fabry disease (FD) is a rare X-linked disease caused by mutations in GLA gene with consequent lysosomal accumulation of globotriaosylceramide (Gb3). globotriaosylceramide alpha 1,4-galactosyltransferase (P blood group) Homo sapiens