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HARVARD Citation
Correia, S. et al. (2021). Severe congenital lactic acidosis and hypertrophic cardiomyopathy caused by an intronic variant in NDUFB7. Human mutation. 42 (4), pp. 378-384. [Online].
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Correia, S. et al. (2021). Severe congenital lactic acidosis and hypertrophic cardiomyopathy caused by an intronic variant in NDUFB7. Human mutation. 42 (4), pp. 378-384. [Online].