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Jonckheere, An I., Huigsloot, Merei, Lammens, Martin ORCID: 0000-0002-3881-6692, Jansen, Jitske, van den Heuvel, Lambert P., Spiekerkoetter, Ute, von Kleist-Retzow, Juergen-Christoph, Forkink, Marleen, Koopman, Werner J. H., Szklarczyk, Radek, Huynen, Martijn A., Fransen, Jack A., Smeitink, Jan A. M. and Rodenburg, Richard J. T.
(2011).
Restoration of complex V deficiency caused by a novel deletion in the human TMEM70 gene normalizes mitochondrial morphology.
Mitochondrion, 11 (6).
S. 954 - 964.
OXFORD:
ELSEVIER SCI LTD.
ISSN 1567-7249
Willems, Esther, Lores-Motta, Laura, Zanichelli, Andrea, Suffritti, Chiara, van der Flier, Michiel, van der Molen, Renate G., Langereis, Jeroen D., van Drongelen, Joris, van den Heuvel, Lambert P., Volokhina, Elena, van de Kar, Nicole C. A. J., Keizer-Garritsen, Jenneke, Levin, Michael ORCID: 0000-0003-2767-6919, Herberg, Jethro A., Martinon-Torres, Federico
ORCID: 0000-0002-9023-581X, Wessels, Hans J. T. C., de Breuk, Anita, Fauser, Sascha, Hoyng, Carel B., den Hollander, Anneke, I, de Groot, Ronald, van Gool, Alain J., Gloerich, Jolein and de Jonge, Marien, I
(2020).
Quantitative multiplex profiling of the complement system to diagnose complement-mediated diseases.
Clin. Transl. Immunol., 9 (12).
HOBOKEN:
WILEY.
ISSN 2050-0068
de Jong, Sarah ORCID: 0000-0002-3705-3371, de Breuk, Anita, Volokhina, Elena B., Bakker, Bjorn, Garanto, Alejandro
ORCID: 0000-0001-5721-1560, Fauser, Sascha, Katti, Suresh, Hoyng, Carel B., Lechanteur, Yara T. E., van den Heuvel, Lambert P. and den Hollander, Anneke, I
(2022).
Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene.
Hum. Mol. Genet., 31 (3).
S. 455 - 471.
OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2083