Fabry disease (FD, OMIM: 301500) is an X-linked inherited lysosomal storage disease (LSD) caused by mutations in the GLA gene that encodes the exogalactosyl hydrolase α-galactosidase A (α-Gal A; GenBank: NP_000160.1) and results in insufficient α-Gal A activity [1]. Here, GLA is linked to Fabry disease.