Phenotypic Characterization of Male <i>Tafazzin</i>-Knockout Mice at 3, 6, and 12 Months of Age
Barth syndrome (BTHS) is an X-linked mitochondrial disease caused by mutations in the gene encoding for tafazzin (<i>TAZ</i>), a key enzyme in the remodeling of cardiolipin. Mice with a germline deficiency in <i>Taz</i> have been generated (<i>Taz</i>-KO) but not yet fully characterized. We performe...
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| Hauptverfasser: | , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
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MDPI AG
2023-02-01
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| Schriftenreihe: | Biomedicines |
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| Online-Zugang: | https://www.mdpi.com/2227-9059/11/2/638 |
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