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Description
Fabry Disease Fabry disease is a genetic disorder caused by a deficiency in lysosomal -galactosidase A, of which neuropathic pain is the hallmark
This pathway is the primary energy source for the heart and a major energy source for skeletal muscle during sustained activity
Carnitine acyltransferases are a family of enzymes responsible for production of acylcarnitines, and among them, they have specificities that cover fatty acids differing in chain-length, branching and other structural features, over the entire range of acyl chain lengths, depending on the cellular location and metabolic purpose, and they enable reversible shuttling of acyl groups between free CoA and carnitine
The genes encoding for these enzymes are positively regulated by the oncogene AKT which acts upstream the transcription factor Nrf2
It supports both physical and cognitive performance by improving energy efficiency in the body
