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HARVARD Citation
Wei, X. et al. (2020). Mutations in FASTKD2 are associated with mitochondrial disease with multi‐OXPHOS deficiency. Human mutation. 41 (5), pp. 961-972. [Online].
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Wei, X. et al. (2020). Mutations in FASTKD2 are associated with mitochondrial disease with multi‐OXPHOS deficiency. Human mutation. 41 (5), pp. 961-972. [Online].