A human importin-beta-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8

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Publication year
2021Source
American Journal of Human Genetics, 108, 6, (2021), pp. 1115-1125ISSN
Publication type
Article / Letter to editor

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Organization
Human Genetics
Journal title
American Journal of Human Genetics
Volume
vol. 108
Issue
iss. 6
Page start
p. 1115
Page end
p. 1125
Subject
All institutes and research themes of the Radboud University Medical Center; Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical NeuroscienceThis item appears in the following Collection(s)
- Academic publications [204996]
- Electronic publications [103288]
- Faculty of Medical Sciences [81051]
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