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HARVARD Citation
Baertling, F. et al. (2018). NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect. Clinical genetics. 93 (1), pp. 111-118. [Online].
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Baertling, F. et al. (2018). NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect. Clinical genetics. 93 (1), pp. 111-118. [Online].