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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)
Research-grade AOD-9604, a synthetic 16-amino-acid peptide fragment (Tyr-hGH 176-191) derived from the C-terminal domain of human growth hormone
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