https://www.selleckchem.com/pr....oducts/gsk2830371.ht
Fabry disease is an X-linked lysosomal storage disorder caused by pathogenic variants in the GLA gene leading to a deficiency of the enzyme alpha-galactosidase A (α-Gal A). Multiple organ systems are implicated in Fabry disease, most severely the cardiac, kidney, and central nervous systems. In this brief review, we will focus on the kidney and central nervous system involvement. There is an urgent clinical need for identifying blood-based diagnostic biomarkers for Dementia with Lewy Bodies (DL. Transcriptomic studies have reported
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