Role of <i>Tafazzin</i> in Mitochondrial Function, Development and Disease
<i>Tafazzin</i>, 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 w...
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| Principais autores: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI AG
2020-05-01
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| coleção: | Journal of Developmental Biology |
| Assuntos: | |
| Acesso em linha: | https://www.mdpi.com/2221-3759/8/2/10 |
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