Heterozygous COL4A3 Variants in Histologically Diagnosed Focal Segmental Glomerulosclerosis-Reference-Cited by-同舟云学术

Heterozygous COL4A3 Variants in Histologically Diagnosed Focal Segmental Glomerulosclerosis

Published:2018-06-12 Issue: Volume:6 Page:
ISSN:2296-2360
Container-title:Frontiers in Pediatrics
language:
Short-container-title:Front. Pediatr.

Author:

Braunisch Matthias C.,Büttner-Herold Maike,Günthner Roman,Satanovskij Robin,Riedhammer Korbinian M.,Herr Pierre-Maurice,Klein Hanns-Georg,Wahl Dagmar,Küchle Claudius,Renders Lutz,Heemann Uwe,Schmaderer Christoph,Hoefele Julia

Publisher

Frontiers Media SA

Subject

Pediatrics, Perinatology, and Child Health

Reference23 articles.

1. Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations;Benoit;Pediatr Nephrol.,2010

2. Familial forms of nephrotic syndrome;Caridi;Pediatr Nephrol.,2010

3. A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome;Sadowski;J Am Soc Nephrol.,2015

4. Focal segmental glomerulosclerosis;D'agati;N Engl J Med.,2011

5. Whole exome sequencing of patients with steroid-resistant nephrotic syndrome;Warejko;Clin J Am Soc Nephrol.,2018

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Case report: A novel compound heterozygous variant in the COL4A3 gene was identified in a patient with autosomal recessive Alport syndrome;Frontiers in Genetics;2024-07-12

2. Is there a dominant‐negative effect in individuals with heterozygous disease‐causing variants in COL4A3/COL4A4?;Clinical Genetics;2024-01-12

3. Hidden genetics behind glomerular scars: an opportunity to understand the heterogeneity of focal segmental glomerulosclerosis?;Pediatric Nephrology;2023-09-20

4. The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy—A human genetics department experience;Frontiers in Medicine;2022-08-31

5. Intravital imaging reveals glomerular capillary distension and endothelial and immune cell activation early in Alport syndrome;JCI Insight;2022-01-11