Barth syndrome(English)
- X-linked disorder characterized by cardiomyopathy, skeletal myopathy, and delayed growth; caused by mutations in the tafazzin gene, which encodes an enzyme involved in the biosynthesis of cardiolipin, a mitochondrial phospholipid
- CMP, DCM, DNAJC19, ETC, HCM, IMM, KSS, mCL, MCU, MELAS, MERRF, MIDD, MLCL, mtDNA, NADH, NRF, OXPHOS, PCr, PDH, PMD, ROS, TAZ, TSH, WPW, β-Ox, MCU, Taz, AICAR, AOX
- Genetics, Enzymes, Cardiology, Musculoskeletal system, Mitochondrion, Myocyte / muscle
- https://www.bar…thsyndrome.html
- https://doi.org…rheartj/ehaf491