Index | PMID | Date | Reference |
---|---|---|---|
1 | 35252560 | 2022 | Hippen, M., Zsurka, G., Peeva, V., Machts, J., Schwiecker, K., Debska-Vielhaber, G., Wiesner, R., Vielhaber, S., Kunz, W. (2022) Novel pathogenic sequence variation m.5789T>C causes NARP syndrome and promotes formation of deletions of the mitochondrial genome Neurology Genetics . 8 (2): e660 . |