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.

Details

Language :

English

ISSN :

2296858X

Database :

Complementary Index

Journal :

Frontiers in Medicine

Publication Type :

Academic Journal

Accession number :

174677592

Full Text :

https://doi.org/10.3389/fmed.2023.1320054