Current Knowledge on the Role of Cardiolipin Remodeling in the Context of Lipid Oxidation and Barth Syndrome

Barth syndrome (BTHS, OMIM 302060) is a genetic disorder caused by variants of the TAFAZZIN gene (G 4.5, OMIM 300394). This debilitating disorder is characterized by cardio- and skeletal myopathy, exercise intolerance, and neutropenia. TAFAZZIN is a transacylase that catalyzes the second step in the...

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Detalles Bibliográficos
Autores principales: Liang, Zhuqing, Schmidtke, Michael W., Greenberg, Miriam L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Molecular Biosciences
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184736/
https://www.ncbi.nlm.nih.gov/pubmed/35693555
http://dx.doi.org/10.3389/fmolb.2022.915301

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184736/
https://www.ncbi.nlm.nih.gov/pubmed/35693555
http://dx.doi.org/10.3389/fmolb.2022.915301

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