Cite
HARVARD Citation
Campbell, T. et al. (2021). Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathy. Human mutation. 42 (2), pp. 177-188. [Online].
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Campbell, T. et al. (2021). Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathy. Human mutation. 42 (2), pp. 177-188. [Online].