Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis – a single-centre experience

Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis – a single-centre experience

The aim of our study was to examine NPHS1, NPHS2, WT1 and LAMB2 mutations, previously reported in two thirds of patients with nephrotic syndrome with onset before the age of one year old. Genomic DNA samples from Polish children (n=33) with Steroid-ResistantNephrotic Syndrome (SRNS) due to focal seg...

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Bibliographic Details
Main Authors: Agnieszka Bińczak-Kuleta, Mieczysław Litwin, Małgorzata Ryder, Klaudyna Lewandowska, Olga Taryma-Leśniak, Jeremy S. Clark, Ryszard Grenda, Andrzej Ciechanowicz
Format: Article
Language:English
Published: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2015-05-01
Series:Bosnian Journal of Basic Medical Sciences
Subjects:
gene variant
NPHS2
WT1
children
steroid-resistant nephrotic syndrome
FSGS
Online Access:https://bjbms.org/ojs/index.php/bjbms/article/view/2270

Internet

https://bjbms.org/ojs/index.php/bjbms/article/view/2270

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