Genotype of PAX2-related disorders correlates with kidney and ocular manifestations
Source: European Journal of Human Genetics
Variable Phenotypic Expression of PAX2 Variants in Two Lithuanian Families with Kidney Disease
Source: Medicina (Lithuania)
No causative variants found': An unusual presentation of PAX2-related disorder not detected on rapid whole exome sequencing testing
Source: BMJ Case Reports
Choroidal neovascularization complicating papillorenal (renal coloboma) syndrome
Source: Journal Francais d'Ophtalmologie
Frameshift Mutation in PAX2 Related to Focal Segmental Glomerular Sclerosis: A Case Report and Literature Review
Source: Molecular Genetics and Genomic Medicine
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