A genetic variant in the NR3C2 gene, encoding the mineralocorticoid receptor, is associated with chronic central serous chorioretinopathy

Author(s):
Schellevis, R.L.; Dijk, E.H.C. van (0000-0002-6351-7942); Bergen, M.G.J.M. van; Breukink, M.B.; Altay, L.; Scholz, P.; Fauser, S.; Meijer, O.C. (0000-0002-8394-6859); Hoyng, C.B.; Hollander, A.I. den; Boon, C.J.F.; Jong, E.K. de
Published
2017
Publication type
Article / Letter to editor
Date issued
2017-04-30
Language
English
Is part of
Acta Ophthalmologica (2017), Vol. 95, p. 21-21
hdl
1887/116517