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 |
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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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