tallózása szerző szerint "Haack, Tobias B"

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  • Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11 
    Reinson, Karit; Kovács-Nagy, Réka; 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 (2019)
    Mitochondrial complex I deficiency is the most frequent mitochondrial disorder presenting in childhood and the mutational spectrum is highly heterogeneous. The NDUFB11 gene is one of the recently identified genes, which ...