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Methods This prospective cohort study analyzed 4,354 adults (45 years) from the China Health and Retirement Longitudinal Study (20112015)

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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)