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Articles

Original Research

Accepted on 24 Nov 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 (FSGS) IS ASSOCIATED WITH A MILDER DISEASE AND ITS UNDERDIAGNOSIS IN CHILDHOOD. Running head: Common founder NPHS2 gene variant c.868G>A in an adult Czech FSGS cohort

in Nephrology

  • Dana Thomasová
  • Michaela Zelinová
  • Malgorzata Libik
  • Jan Geryk
  • Pavel Votýpka
  • Silvie Rajnochová Bloudíčkova
  • Karel Krejčí
  • Jana Reiterová
  • Eva Jancova
  • Jana Machová
Frontiers in Medicine
doi 10.3389/fmed.2023.1320054