Larsson, N.G. Department Larsson - Mitochondrial Biology, Max Planck Institute for Biology of Ageing, Max Planck Society;
Lesko, N., Naess, K., Wibom, R., Solaroli, N., Nennesmo, I., von Dobeln, U., Karlsson, A., & Larsson, N. (2010). Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion. Neuromuscul Disord, 20(3), 198-203. doi:10.1016/j.nmd.2009.11.013.