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Title: Disruption of the Basal Body Protein POC1B Results in Autosomal-Recessive Cone-Rod Dystrophy
Author(s): Roosing, S. ; Lamers, I.J.C.; Vrieze, E. de ; Born, L.I. van den; Lambertus, S.; Arts, H.H. ; Peters, T.A. ; Hoyng, C.B. ; Kremer, H. ; Hetterschijt, L. ; Letteboer, S.J. ; Wijk, H.A.R. van ; Roepman, R. ; Hollander, A.I. den ; Cremers, F.P.M. ; et al.
Publication year: 2014
Source: American Journal of Human Genetics, vol. 95, iss. 2, (2014), pp. 131-142
ISSN: 0002-9297
DOI: https://doi.org/10.1016/j.ajhg.2014.06.012
Publication type: Article / Letter to editor

Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/137801   http://hdl.handle.net/2066/137801

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Subject: Radboudumc 11: Renal disorders RIMLS: Radboud Institute for Molecular Life Sciences
Radboudumc 12: Sensory disorders RIHS: Radboud Institute for Health Sciences
Radboudumc 12: Sensory disorders RIMLS: Radboud Institute for Molecular Life Sciences
Organization: Ophthalmology
Human Genetics
Otorhinolaryngology
Journal title:
American Journal of Human Genetics
Volume: vol. 95
Issue: iss. 2
Page start: p. 131
Page end: p. 142

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