Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic Counseling
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Publisher’s version
Publication year
2019Source
American Journal of Kidney Diseases, 73, 3, (2019), pp. 400-403ISSN
Publication type
Article / Letter to editor
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Organization
Nephrology
Human Genetics
Paediatrics
Journal title
American Journal of Kidney Diseases
Volume
vol. 73
Issue
iss. 3
Page start
p. 400
Page end
p. 403
Subject
Radboudumc 11: Renal disorders RIHS: Radboud Institute for Health Sciences; Radboudumc 12: Sensory disorders DCMN: Donders Center for Medical Neuroscience; Radboudumc 9: Rare cancers RIHS: Radboud Institute for Health Sciences; Human Genetics - Radboud University Medical Center; Nephrology - Radboud University Medical Center; Paediatrics - Radboud University Medical Center; Radboud University Medical CenterThis item appears in the following Collection(s)
- Academic publications [242524]
- Electronic publications [129515]
- Faculty of Medical Sciences [92283]
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