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Torraco, A. et al. (2021). Novel NDUFA12 variants are associated with isolated complex I defect and variable clinical manifestation. Human mutation. 42 (6), pp. 699-710. [Online].
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Torraco, A. et al. (2021). Novel NDUFA12 variants are associated with isolated complex I defect and variable clinical manifestation. Human mutation. 42 (6), pp. 699-710. [Online].