De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment
SourceHuman Genetics, 138, 1, (2019), pp. 61-72
Article / Letter to editor
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SubjectAll 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 Sciences
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