A Drosophila model of mitochondrial disease caused by a complex I mutation that uncouples proton pumping from electron transfer

© 2014, Company of Biologists Ltd. All rights reserved. Mutations affecting mitochondrial complex I, a multi-subunit assembly that couples electron transfer to proton pumping, are the most frequent cause of heritable mitochondrial diseases. However, the mechanisms by which complex I dysfunction resu...

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Main Authors: Jonathon L. Burman, Leslie S. Itsara, Ernst Bernhard Kayser, Wichit Suthammarak, Adrienne M. Wang, Matt Kaeberlein, Margaret M. Sedensky, Philip G. Morgan, Leo J. Pallanck
其他作者: University of Washington, Seattle
格式: Article
出版: 2018
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在線閱讀:https://repository.li.mahidol.ac.th/handle/123456789/33459
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機構: Mahidol University

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