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HARVARD Citation
Kishita, Y. et al. (2021). Genome sequencing and RNA‐seq analyses of mitochondrial complex I deficiency revealed Alu insertion‐mediated deletion in NDUFV2. Human mutation. 42 (11), pp. 1422-1428. [Online].
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Kishita, Y. et al. (2021). Genome sequencing and RNA‐seq analyses of mitochondrial complex I deficiency revealed Alu insertion‐mediated deletion in NDUFV2. Human mutation. 42 (11), pp. 1422-1428. [Online].