De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment
Publication year
2019Source
Human Genetics, 138, 1, (2019), pp. 61-72ISSN
Publication type
Article / Letter to editor
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Organization
Human Genetics
Otorhinolaryngology
Journal title
Human Genetics
Volume
vol. 138
Issue
iss. 1
Page start
p. 61
Page end
p. 72
Subject
All institutes and research themes of the Radboud University Medical Center; Radboudumc 12: Sensory disorders DCMN: Donders Center for Medical Neuroscience; Radboudumc 9: Rare cancers RIHS: Radboud Institute for Health SciencesThis item appears in the following Collection(s)
- Academic publications [238441]
- Electronic publications [122523]
- Faculty of Medical Sciences [90373]
- Open Access publications [97518]
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