Feasibility of flow cytometric analysis of the mitochondrial energy metabolism in fibroblasts and peripheral blood

NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals with Leigh-like Encephalomyopathy.

Piekutowska-Abramczuk, D., Assouline, Z., Mataković, L., Feichtinger, R. (Co-Autor/-in), Koňařiková, E., Jurkiewicz, E., Stawiński, P., Gusic, M., Koller, A. (Co-Autor/-in), Pollak, A., Gasperowicz, P., Trubicka, J., Ciara, E., Iwanicka-Pronicka, K., Rokicki, D., Hanein, S., Wortmann, S. (Co-Autor/-in), Sperl, W. (Co-Autor/-in), Rötig, A. & Prokisch, H. &4 mehr, Pronicka, E., Płoski, R., Barcia, G. & Mayr, J. A. (Letztautor/-in), 2018, in: AMERICAN JOURNAL OF HUMAN GENETICS . 102, 3, S. 460-467

Publikation: Beitrag in Fachzeitschrift › Originalarbeit › Begutachtung