Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease

Natalie Keller(University of Cologne), Mert Karakaya(University of Cologne), Uluç Yiş(Dokuz Eylül University), Cem Paketçi(Dokuz Eylül University), Hölger Thiele(Leipzig Heart Institute), Brunhilde Wirth(University of Cologne), Susanne Motameny(University of Cologne), Olcay Ünver(Marmara University), Ehsan Ghayoor Karimiani(St George's, University of London), Sanem Yılmaz(Ege University), Peter Nürnberg(Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases), Reza Boostani(Mashhad University of Medical Sciences), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Nico Fuhrmann(University of Cologne), Gilbert Wunderlich(University Hospital Cologne), Janine Altmueller(University of Cologne), Bertold Schrank(Helios Kliniken)
Human Mutation
February 18, 2021
Cited by 10


Related Papers