Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11
Titel:
Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11
Auteur:
Reinson, Karit Kovacs-Nagy, Reka Õiglane-Shlik, Eve Pajusalu, Sander Nõukas, Margit Wintjes, Liesbeth T. van den Brandt, Frans C.A. Brink, Maaike Acker, Till Ahting, Uwe Hahn, Andreas Schänzer, Anne Haack, Tobias B. Rodenburg, Richard J. Õunap, Katrin