Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy
Publication year
2018Source
Journal of Immunology, 200, 7, (2018), pp. 2464-2478ISSN
Publication type
Article / Letter to editor
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Organization
Paediatrics
Laboratory Medicine
Journal title
Journal of Immunology
Volume
vol. 200
Issue
iss. 7
Page start
p. 2464
Page end
p. 2478
Subject
Radboudumc 11: Renal disorders RIMLS: Radboud Institute for Molecular Life Sciences; Laboratory Medicine - Radboud University Medical Center; Paediatrics - Radboud University Medical Center; Radboud University Medical CenterThis item appears in the following Collection(s)
- Academic publications [246165]
- Faculty of Medical Sciences [93268]
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