Barth Syndrome: Exploring Cardiac Metabolism with Induced Pluripotent Stem Cell-Derived Cardiomyocytes

Barth syndrome (BTHS) is an X-linked recessive multisystem disorder caused by mutations in the TAZ gene (TAZ, G 4.5, OMIM 300394) that encodes for the acyltransferase tafazzin. This protein is highly expressed in the heart and plays a significant role in cardiolipin biosynthesis. Heart disease is th...

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Detalles Bibliográficos
Autores principales: Fatica, Erica M., DeLeonibus, Gina A., House, Alisha, Kodger, Jillian V., Pearce, Ryan W., Shah, Rohan R., Levi, Liraz, Sandlers, Yana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6950123/
https://www.ncbi.nlm.nih.gov/pubmed/31861102
http://dx.doi.org/10.3390/metabo9120306

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6950123/
https://www.ncbi.nlm.nih.gov/pubmed/31861102
http://dx.doi.org/10.3390/metabo9120306

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