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Role of Tafazzin in Mitochondrial Function, Development and Disease
Tafazzin, an enzyme associated with the rare inherited x-linked disorder Barth Syndrome, is a nuclear encoded mitochondrial transacylase that is highly conserved across multiple species and plays an important role in mitochondrial function. Numerous studies have elucidated the mechanisms by which Ta...
Autores principales: | Chin, Michael T., Conway, Simon J. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344621/ https://www.ncbi.nlm.nih.gov/pubmed/32456129 http://dx.doi.org/10.3390/jdb8020010 |
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