Correction of the Splicing Defect Caused by a Recurrent Variant in ABCA4 (c.769-784C>T) That Underlies Stargardt Disease
Publication year
2022Source
Cells, 11, 24, (2022), article 3947ISSN
Publication type
Article / Letter to editor
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Organization
Human Genetics
Paediatrics
Journal title
Cells
Volume
vol. 11
Issue
iss. 24
Subject
Radboudumc 12: Sensory disorders DCMN: Donders Center for Medical Neuroscience; Radboudumc 6: Metabolic Disorders RIMLS: Radboud Institute for Molecular Life Sciences; Paediatrics - Radboud University Medical Center; Radboud University Medical CenterThis item appears in the following Collection(s)
- Academic publications [244228]
- Electronic publications [131195]
- Faculty of Medical Sciences [92893]
- Open Access publications [105220]
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