CASE REPORT
Accepted on 28 Feb 2025
Case Report: A Novel Splice Variant in WT1 Leads to Focal Segmental Glomerulosclerosis and Uterine Anomalies through Exon Skipping
doi 10.3389/fneph.2025.1542475
- Frontiers in Nephrology
- Glomerular disease
- Research Topics
- Mechanistic Insights in Hereditary Kidney Disease
Mechanistic Insights in Hereditary Kidney Disease
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Articles
REVIEW
Published on 16 Jan 2024
Primary cilia and actin regulatory pathways in renal ciliopathies
doi 10.3389/fneph.2023.1331847
- 3,691 views
- 3 citations
REVIEW
Published on 20 Apr 2023
Hedgehog-GLI mediated control of renal formation and malformation
doi 10.3389/fneph.2023.1176347
- 1,646 views
- 4 citations
BRIEF RESEARCH REPORT
Published on 23 Sep 2022
Outcomes from the Northeast England cohort of autosomal dominant polycystic kidney disease (ADPKD) patients on tolvaptan
doi 10.3389/fneph.2022.984165
- 1,566 views
- 2 citations
