Familial focal segmental glomerulosclerosis with PLCE 1 mutation in siblings-Reference-Cited by-同舟云学术

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Familial focal segmental glomerulosclerosis with PLCE 1 mutation in siblings

Published:2019-07 Issue:7 Volume:61 Page:726-727
ISSN:1328-8067
Container-title:Pediatrics International
language:en
Short-container-title:Pediatrics International

Author:

Shimizu Masaki¹^ORCID,Irabu Hitoshi¹,Kaneda Hisashi²,Ohta Kazuhide³,Nozu Kandai⁴

Affiliation:

1. Department of Pediatrics School of Medicine Institute of Medical, Pharmaceutical and Health Sciences Kanazawa University Kanazawa, Ishikawa Japan

2. Department of Pediatrics Kanazawa Medical Center Kanazawa Ishikawa Japan

3. Department of Pediatrics Komatsu Municipal Hospital Komatsu, IshikawaJapan

4. Department of Pediatrics Kobe University Graduate School of Medicine Kobe Hyogo Japan

Publisher

Wiley

Subject

Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ped.13870

Reference5 articles.

1. Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

2. Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)

3. Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome

4. A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome

5. Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis

Cited by 2 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. A broad clinical spectrum of PLCε1-related kidney disease and intrafamilial variability;Pediatric Nephrology;2022-01-16

2. Crumbs homolog 2 mutation in two siblings with steroid-resistant nephrotic syndrome: Two case reports;World Journal of Clinical Cases;2021-05-06

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