Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis – a single-centre experience-Reference-Cited by-同舟云学术

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

Published:2015-05-20 Issue:2 Volume:14 Page:89
ISSN:1840-4812
Container-title:Bosnian Journal of Basic Medical Sciences
language:
Short-container-title:Bosn J of Basic Med Sci

Author:

Bińczak-Kuleta Agnieszka,Litwin Mieczysław,Ryder Małgorzata,Lewandowska Klaudyna,Taryma-Leśniak Olga,S. Clark Jeremy,Grenda Ryszard,Ciechanowicz Andrzej

Publisher

Association of Basic Medical Sciences of FBIH

Subject

General Medicine

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa;European Journal of Pediatrics;2022-08-03

2. Spectrum of Clinical Manifestations in Children With WT1 Mutation: Case Series and Literature Review;Frontiers in Pediatrics;2022-04-15

3. Identification of Nephrin gene variants in Indian children associated with Steroid sensitive and Steroid resistant nephrotic syndrome;Meta Gene;2022-02

4. Systematic Review of Genotype-Phenotype Correlations in Frasier Syndrome;Kidney International Reports;2021-10

5. Mutational landscape of TRPC6, WT1, LMX1B, APOL1, PTPRO, PMM2, LAMB2 and WT1 genes associated with Steroid resistant nephrotic syndrome;Molecular Biology Reports;2021-09-21

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