Whole-exome sequencing in pediatric patients with glomerulonephritis

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Authors

Marina Perić · Institute of Public Health of Serbia

Marija Branković · University Children's Hospital, Belgrade

Nataša Stajić · Institute of Public Health of Serbia

Jovana Putnik · University of Belgrade

Aleksandra Paripović · University of Belgrade

Milena Janković · Centar za Promociju Nauke

Dejan Nikolić

Abstract

WES helped us detect hereditary diseases that have a clinical presentation like GN, including Alport syndrome and possible aHUS. Finding susceptibility genes in GN helped us understand disease pathophysiology.

Topics & Keywords

Renal Diseases and Glomerulopathies Genomics and Rare Diseases Complement system in diseases

Publication Details

Published in: Frontiers in Genetics

Volume 16, pp. 1611340-1611340

DOI: 10.3389/fgene.2025.1611340

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Whole-exome sequencing in pediatric patients with glomerulonephritis

Authors

Abstract

Topics & Keywords

Publication Details