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1887
94673
Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by Pseudocoloboma
Author(s):
Pierrache, L.H.M.; Kimchi, A.; Ratnapriya, R.; Roberts, L.; Astuti, G.D.N.; Obolensky, A.; Beryozkin, A.; Tjon-Fo-Sang, M.J.H.; Schuil, J.; Klaver, C.C.W.; Bongers, E.M.H.F.; Haer-Wigman, L.; Schalij, N.; Breuning, M.H. (
0000-0002-8212-4319
); Fischer, G.M.; Banin, E.; Ramesar, R.S.; Swaroop, A.; Born, L.I. van den; Sharon, D.; Cremers, F.P.M.
Published
2017
Publication type
Article / Letter to editor
Date issued
2017-07-31
Language
English
Is part of
Ophthalmology: Journal of The American Academy of Ophthalmology (2017), Vol. 124, no. 7, p. 992-1003
hdl
1887/94673
doi
10.1016/j.ophtha.2017.03.010
Persistent identifier url
https://hdl.handle.net/1887/94673
Documents
01 - 10.1016-j.ophtha.2017.03.010
version: Not Applicable (or Unknown)
Open Access