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Barth syndrome: connecting cardiolipin to cardiomyopathy
Barth syndrome (BTHS) is caused by an inborn error of metabolism that manifests characteristic phenotypic features including altered mitochondrial membrane phospholipids, lactic acidosis, organic acid-uria, skeletal muscle weakness and cardiomyopathy. The underlying cause of BTHS has been definitive...
Guardado en:
| Publicado en: | Lipids |
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| Autores principales: | , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2017
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5288132/ https://ncbi.nlm.nih.gov/pubmed/28070695 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11745-016-4229-7 |
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