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Mitochondrial dysfunctions in Barth syndrome
Barth syndrome (BTHS) is a rare, multi-systemic genetic disorder caused by mutations in the TAZ gene. TAZ encodes a mitochondrial enzyme that remodels the acyl chain composition of newly synthesized cardiolipin, a phospholipid unique to mitochondrial membranes. The clinical abnormalities observed in...
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| Publicado no: | IUBMB Life |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6586490/ https://ncbi.nlm.nih.gov/pubmed/30746873 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/iub.2018 |
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