Steroid-resistant nephrotic syndrome in infants caused by a novel compound heterozygous mutation of the NUP93-Reference-Cited by-同舟云学术

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Steroid-resistant nephrotic syndrome in infants caused by a novel compound heterozygous mutation of the NUP93

Published:2021-02-12 Issue:6 Volume:100 Page:e24627
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Zhao Bo,Chen Ji-Yu,Liao Ya-Bin,Li Yan-Fang,Jiang Xue-Mei,Bi Xin,Yang Mi-Feng,Li Li,Cui Jing-Jing

Funder

the Joint Special Fund for Basic Research from Yunnan Provincial Science and Technology Department and Kunming Medical University

Kunming Research Center for Blood Purification in Children

Kunming Health Science and Technology Talent Project-100 Projects

the National Natural Science Foundation of China

the Basic Applied Study Planning Projects of Yunnan Province

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference23 articles.

1. Nephrotic syndrome in childhood;Eddy;Lancet,2003

2. Nephrotic syndrome in children;Lennon;Paediatr Child Health,2012

3. Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort;Trautmann;Clin J Am Soc Nephrol,2015

4. Genetics of childhood steroid-sensitive nephrotic syndrome;Karp;Pediatr Nephrol,2017

5. A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome;Sadowski;J Am Soc Nephrol,2015

Cited by 6 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. Mutations in the NUP93, NUP107 and NUP160 genes cause steroid-resistant nephrotic syndrome in Chinese children;Italian Journal of Pediatrics;2024-04-22

2. From the sideline: Tissue‐specific nucleoporin function in health and disease, an update;FEBS Letters;2023-11

3. Steroid-Resistant Nephrotic Syndrome Caused by NUP93 Pathogenic Variants;Journal of Clinical Medicine;2023-09-07

4. A rare cause of steroid-resistant nephrotic syndrome – a case report;Central European Journal of Immunology;2023

5. Mutation in XPO5 causes adult-onset autosomal dominant familial focal segmental glomerulosclerosis;Human Genomics;2022-11-12

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