Elevated liver glycogenolysis mediates higher blood glucose during acute exercise in Barth syndrome

Barth syndrome (BTHS) is an X-linked recessive genetic disorder due to mutations in the Tafazzin (TAFAZZIN) gene that lead to cardiac and skeletal muscle mitochondrial dysfunction. Previous studies in humans with BTHS demonstrate that the defects in muscle mitochondrial oxidative metabolism result i...

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Detalles Bibliográficos
Autores principales: Schweitzer, George G., Ditzenberger, Grace L., Hughey, Curtis C., Finck, Brian N., Martino, Michael R., Pacak, Christina A., Byrne, Barry J., Cade, William Todd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470866/
https://www.ncbi.nlm.nih.gov/pubmed/37651450
http://dx.doi.org/10.1371/journal.pone.0290832

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470866/
https://www.ncbi.nlm.nih.gov/pubmed/37651450
http://dx.doi.org/10.1371/journal.pone.0290832

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