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

Project: Research

Status	Finished
Effective start/end date	1/06/17 → 1/06/18

NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals with Leigh-like Encephalomyopathy.
Piekutowska-Abramczuk, D., Assouline, Z., Mataković, L., Feichtinger, R. (Co-author), Koňařiková, E., Jurkiewicz, E., Stawiński, P., Gusic, M., Koller, A. (Co-author), Pollak, A., Gasperowicz, P., Trubicka, J., Ciara, E., Iwanicka-Pronicka, K., Rokicki, D., Hanein, S., Wortmann, S. (Co-author), Sperl, W. (Co-author), Rötig, A. & Prokisch, H. & 4 others, Pronicka, E., Płoski, R., Barcia, G. & Mayr, J. A. (Last author), 2018, In: AMERICAN JOURNAL OF HUMAN GENETICS . 102, 3, p. 460-467
Research output: Contribution to journal › Original Article › peer-review

43 Citations (Web of Science)

Project Details