Original Research
Published on 19 Dec 2023
The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated with a milder disease and its underdiagnosis in childhood
in Nephrology
Frontiers in Medicine
doi 10.3389/fmed.2023.1320054
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