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Keller, N. et al. (2021). Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease. Human mutation. 42 (4), pp. 460-472. [Online].
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Keller, N. et al. (2021). Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease. Human mutation. 42 (4), pp. 460-472. [Online].