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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...
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| 出版年: | J Dev Biol |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7344621/ https://ncbi.nlm.nih.gov/pubmed/32456129 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jdb8020010 |
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