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Published in 2018 at "Mitochondrion"
DOI: 10.1016/j.mito.2018.10.005
Abstract: Mutations in the tafazzin gene are the basis of Barth syndrome. The tafazzin protein is responsible for the synthesis of cardiolipin. Doxycycline-induced tafazzin-knockdown mice have been used as a model for Barth syndrome. In the…
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Keywords:
tafazzin knockdown;
knockdown mice;
barth syndrome;
cardiac mitochondrial ... See more keywords