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Dive into the research topics of 'Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect'. Together they form a unique fingerprint.- Sort by
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H. Antonicka, E. Ostergaard, F. Sasarman, W. Weraarpachai, F. Wibrand, A.M.B. Pedersen, R.J. Rodenburg, M.S. van der Knaap, J.A.M. Smeitink, ZM Chrzanowska-Lightowlers, E.A. Shoubridge
Research output: Contribution to Journal › Article › Academic › peer-review