Cite
APA Citation
Keller, N., Paketci, C., Altmueller, J., Fuhrmann, N., Wunderlich, G., Schrank, B., Unver, O., Yilmaz, S., Boostani, R., Karimiani, E. G., Motameny, S., Thiele, H., Nürnberg, P., Maroofian, R., Yis, U., Wirth, B., & Karakaya, M. (2021). genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease. Human mutation, 42(4), 460–472. http://access.bl.uk/ark:/81055/vdc_100127492990.0x00002d