Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+11655A > G Mutation in CEP290
Publication year
2018Source
Investigative Ophthalmology and Visual Science, 59, 11, (2018), pp. 4384-4391ISSN
Publication type
Article / Letter to editor

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Organization
Ophthalmology
Human Genetics
Journal title
Investigative Ophthalmology and Visual Science
Volume
vol. 59
Issue
iss. 11
Page start
p. 4384
Page end
p. 4391
Subject
All institutes and research themes of the Radboud University Medical Center; Radboudumc 12: Sensory disorders DCMN: Donders Center for Medical NeuroscienceThis item appears in the following Collection(s)
- Academic publications [232155]
- Electronic publications [115338]
- Faculty of Medical Sciences [89071]
- Open Access publications [82661]
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