作者: S.J. Annesley , S. Chen , L.M. Francione , O. Sanislav , A.J. Chavan
DOI: 10.1016/J.BBAGEN.2013.10.019
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摘要: Background Most neurodegenerative diseases are associated with mitochondrial dysfunction. In humans, mutations in mitochondrial genes result in a range of phenotypic outcomes …