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Number of items: 3.

Journal Article

Geerlings, Maartje J., Kremlitzka, Mariann, Bakker, Bjorn, Nilsson, Sara C., Saksens, Nicole T., Lechanteur, Yara T., Pauper, Marc ORCID: 0000-0001-6274-9891, Corominas, Jordi, Fauser, Sascha, Hoyng, Carel B., Blom, Anna M., de Jong, Eiko K. and den Hollander, Anneke I. (2017). The Functional Effect of Rare Variants in Complement Genes on C3b Degradation in Patients With Age-Related Macular Degeneration. JAMA Ophthalmol., 135 (1). S. 39 - 47. CHICAGO: AMER MEDICAL ASSOC. ISSN 2168-6173

Kremlitzka, Mariann, Geerlings, Maartje J., de Jong, Sarah, Bakker, Bjorn, Nilsson, Sara C., Fauser, Sascha, Hoyng, Carel B., de Jong, Eiko K., den Hollander, Anneke I. and Blom, Anna M. (2018). Functional analyses of rare genetic variants in complement component C9 identified in patients with age-related macular degeneration. Hum. Mol. Genet., 27 (15). S. 2678 - 2689. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2083

Kremlitzka, Mariann, de Jong, Sarah, Geerlings, Maartje ORCID: 0000-0003-1164-3573, Bakker, Bjorn, Nilsson, Sara C., Fauser, Sascha, Hoyng, Carel B., de Jong, Eiko K., den Hollander, Anneke I. and Blom, Anna M. (2017). Functional analysis of AMD-associated rare genetic variants in C9. Mol. Immunol., 89. S. 150 - 151. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 0161-5890

This list was generated on Tue Jan 19 04:09:55 2021 CET.