Cardiolipin deficiency in Barth syndrome is not associated with increased superoxide/H2 O2 production in heart and skeletal muscle mitochondria. Author(s): Goncalves RLS, Schlame M, Bartelt A, Brand MD, Hotamisligil GS|Journal: FEBS Lett|PMID: 33112430| October 2020 Barth syndrome (BTHS) is a rare X-linked genetic disorder caused by mutations in the gene encoding the transacylase tafazzin and…
