Characterization of a novel disease-associated mutation within NPHS1 and its effects on nephrin phosphorylation and signaling
Author:
Funder
Canadian Institutes of Health Research
Canada Research Chairs
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
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4. NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described;MS Guaragna;Nephrology,2016
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