No causative variants found': An unusual presentation of PAX2-related disorder not detected on rapid whole exome sequencing testing
Source: BMJ Case Reports
Frameshift Mutation in PAX2 Related to Focal Segmental Glomerular Sclerosis: A Case Report and Literature Review
Source: Molecular Genetics and Genomic Medicine
Renal coloboma syndrome/dominant optic atrophy with severe retinal atrophy and de novo digenic mutations in PAX2 and OPA1
Source: Pediatric Nephrology
Familial focal segmental glomerulosclerosis with Alport-like glomerular basement changes caused by paired box protein 2 gene variant
Source: CEN Case Reports
The multifaceted links between hearing loss and chronic kidney disease
Source: Nature Reviews Nephrology
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