1. Novel Pathogenic Sequence Variation m.5789T>C Causes NARP Syndrome and Promotes Formation of Deletions of the Mitochondrial Genome. (3rd April 2022) Authors: Hippen, Marius; Zsurka, Gábor; Peeva, Viktoriya; Machts, Judith; Schwiecker, Kati; Debska-Vielhaber, Grazyna; Wiesner, Rudolf J.; Vielhaber, Stefan; Kunz, Wolfram S. Journal: Neurology Issue: Volume 8:Number 2(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗