The Cardiolipin Transacylase, Tafazzin, Associates with Two Distinct Respiratory Components Providing Insight into Barth Syndrome

Mutations in the mitochondrial cardiolipin (CL) transacylase, tafazzin (Taz1p), result in the X-linked cardioskeletal myopathy, Barth syndrome (BTHS). The mitochondria of BTHS patients exhibit variable respiratory defects and abnormal cristae ultrastructure. The biochemical basis for these observati...

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Hlavní autoři: Claypool, Steven M., Boontheung, Pinmanee, McCaffery, J. Michael, Loo, Joseph A., Koehler, Carla M.
Médium: Artigo
Jazyk:Inglês
Vydáno: The American Society for Cell Biology 2008
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Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2592642/
https://ncbi.nlm.nih.gov/pubmed/18799610
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E08-09-0896
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