Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2
Publication year
2018Source
European Journal of Human Genetics, 26, 1, (2018), pp. 94-106ISSN
Publication type
Article / Letter to editor
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Organization
Neurology
Journal title
European Journal of Human Genetics
Volume
vol. 26
Issue
iss. 1
Page start
p. 94
Page end
p. 106
Subject
Radboudumc 3: Disorders of movement DCMN: Donders Center for Medical Neuroscience; Neurology - Radboud University Medical Center; Radboud University Medical CenterThis item appears in the following Collection(s)
- Academic publications [246860]
- Electronic publications [134292]
- Faculty of Medical Sciences [93474]
- Open Access publications [107812]
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