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Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type

, Savolainen E, et al. Congenital Nephrotic Syndrome of the Finnish Type Maps to the Long Arm of Chromosome 19. Am J Hum Genet 1994;54:757-64.         [ Links ]     Correspondence: Sonbol Ameli, Tehran

NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome

.         [ Links ]     Correspondence: Sonbol Ameli, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran E-mail: E-mail: Enviado a Revisar