Pub. Date : 2021 Feb 2
PMID : 33531072
1 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
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 |