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Schellevis, R. L., van Dijk, E. H. C., van Bergen, M. G. J. M., Breukink, M. B., Altay, L., Scholz, P., Fauser, S., Meijer, O. C., Hoyng, C. B., den Hollander, A. I., Boon, C. J. F. and de Jong, E. K. (2017). A genetic variant in the NR3C2 gene, encoding the mineralocorticoid receptor, is associated with chronic central serous chorioretinopathy. Acta Ophthalmol., 95. S. 21 - 22. HOBOKEN: WILEY. ISSN 1755-3768