Variable renal phenotype in a family with an INF2 mutation-Reference-Cited by-同舟云学术

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Variable renal phenotype in a family with an INF2 mutation

Published:2010-08-28 Issue:1 Volume:26 Page:73-76
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Lee Hyun Kyung,Han Kyoung Hee,Jung Yun Hye,Kang Hee Gyung,Moon Kyung Chul,Ha Il Soo,Choi Yong,Cheong Hae Il

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00467-010-1644-5.pdf

Reference13 articles.

1. Löwik MM, Groenen PJ, Levtchenko EN, Monnens LA, van den Heuvel LP (2009) Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis—a review. Eur J Pediatr 168:1291–1304

2. Machuca E, Benoit G, Antignac C (2009) Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology. Hum Mol Genet 18:R185–R194

3. Tryggvason K, Patrakka J, Wartiovaara J (2006) Hereditary proteinuria syndromes and mechanisms of proteinuria. N Engl J Med 354:1387–1401

4. Hildebrandt F (2010) Genetic kidney diseases. Lancet 375:1287–1295

5. Hinkes BG, Mucha B, Vlangos CN, Gbadegesin R, Liu J, Hasselbacher K, Hangan D, Ozaltin F, Zenker M, Hildebrandt F, members of the Arbeitsgemeinschaft für Pädiatrische Nephrologie Study Group (2007) Nephrotic syndrome in the first year of life: two-thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2). Pediatrics 119:e907–e919

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2. INF2 and ROBO2 gene mutation in an Indian family with end stage renal failure and follow‐up of renal transplantation;Nephrology;2023-09-29

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5. Degree of foot process effacement in patients with genetic focal segmental glomerulosclerosis: a single-center analysis and review of the literature;Scientific Reports;2021-06-08

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