Targeted Overexpression of Catalase in Mitochondria Does Not Prevent Cardioskeletal Myopathy in Barth Syndrome

Barth Syndrome (BTHS) is an X-linked recessive disorder characterized by cardiomyopathy and muscle weakness. The underlying cause of BTHS is a mutation in the tafazzin (TAZ) gene, a key enzyme of cardiolipin biosynthesis. The lack of CL arising from loss of TAZ function results in destabilization of...

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Publicado no:J Mol Cell Cardiol
Main Authors: Johnson, Jordan M., Ferrara, Patrick J., Verkerke, Anthony R. P., Coleman, Chanel B., Wentzler, Edward J., Neufer, P. Darrell, Kew, Kimberly A., de Castro Brás, Lisandra E., Funai, Katsuhiko
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6178222/
https://ncbi.nlm.nih.gov/pubmed/30008435
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yjmcc.2018.07.001
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