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

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Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Schellevis, R. L.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
van Dijk, E. H. C.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
van Bergen, M. G. J. M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Breukink, M. B.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Altay, L.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Scholz, P.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Fauser, S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Meijer, O. C.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hoyng, C. B.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
den Hollander, A. I.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Boon, C. J. F.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
de Jong, E. K.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-235443
Journal or Publication Title: Acta Ophthalmol.
Volume: 95
Page Range: S. 21 - 22
Date: 2017
Publisher: WILEY
Place of Publication: HOBOKEN
ISSN: 1755-3768
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
OphthalmologyMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/23544

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