Novel Pathogenic Sequence Variation m.5789T>C Causes NARP Syndrome and Promotes Formation of Deletions of the Mitochondrial Genome
Hippen, Marius, Zsurka, Gábor, Peeva, Viktoriya, Machts, Judith, Schwiecker, Kati, Debska-Vielhaber, Grazyna, Wiesner, Rudolf J, Vielhaber, Stefan, Kunz, Wolfram S
Published in Neurology. Genetics (01.04.2022)
Published in Neurology. Genetics (01.04.2022)
Get full text
Journal Article