Phenotypic Characterization of Male Tafazzin-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 (TAZ), a key enzyme in the remodeling of cardiolipin. Mice with a germline deficiency in Taz have been generated (Taz-KO) but not yet fully characterized. We performed physiological asses...

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Detalles Bibliográficos
Autores principales: Tomczewski, Michelle V., Chan, John Z., Campbell, Zurie E., Strathdee, Douglas, Duncan, Robin E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953241/
https://www.ncbi.nlm.nih.gov/pubmed/36831174
http://dx.doi.org/10.3390/biomedicines11020638

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953241/
https://www.ncbi.nlm.nih.gov/pubmed/36831174
http://dx.doi.org/10.3390/biomedicines11020638

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