Keller, N. Et Al. 2021. Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease. HUMAN MUTATION , vol.42, no.4 , 460-472.

Keller, N., Paketci, C., Altmueller, J., Fuhrmann, N., Wunderlich, G., Schrank, B., ... ÜNVER, O.(2021). Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease. HUMAN MUTATION , vol.42, no.4, 460-472.

Keller, Natalie Et Al. "Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease," HUMAN MUTATION , vol.42, no.4, 460-472, 2021

Keller, Natalie Et Al. "Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease." HUMAN MUTATION , vol.42, no.4, pp.460-472, 2021

Keller, N. Et Al. (2021) . "Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease." HUMAN MUTATION , vol.42, no.4, pp.460-472.

@article{article, author={Natalie Keller Et Al. }, title={Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease}, journal={HUMAN MUTATION}, year=2021, pages={460-472} }