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Description
Barth syndrome (BTHS) is a rare X-linked recessively inherited disorder caused by variants in the TAFAZZIN gene, leading to impaired conversion of monolysocardiolipin (MLCL) into mature cardiolipin (CL)
It enhances protein synthesis, supports recovery from injury, and may improve energy expenditure by increasing GH levels, which stimulate insulin-like growth factor-1 (IGF-1) production in the liver
How do they compare
a bioregulator studied for gene expression in aging cells
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Mineral Bioactive Factor 1200mg
