Hippen, Marius
[Author];
Zsurka, Gábor
[Author];
Peeva, Viktoriya
[Author];
Wesenberg, Judith
[Author];
Schwiecker, Kati
[Author];
Debska-Vielhaber, Grazyna
[Author];
Wiesner, Rudolf J.
[Author];
Vielhaber, Stefan
[Author];
Kunz, Wolfram S.
[Author]
Novel pathogenic sequence variation m.5789T>C causes NARP syndrome and promotes formation of deletions of the mitochondrial genome