Parental Whole-Exome Sequencing Enables Sialidosis Type II Diagnosis due to an NEU1 Missense Mutation as an Underlying Cause of Nephrotic Syndrome in the Child
SourceKidney International Reports, 3, 6, (2018), pp. 1454-1463
Article / Letter to editor
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Kidney International Reports
SubjectAll institutes and research themes of the Radboud University Medical Center; Radboudumc 11: Renal disorders RIMLS: Radboud Institute for Molecular Life Sciences
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