Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome

Mutations in the NPHS1, NPHS2, LAMB2, and the WT1 genes are responsible for causing nephrotic syndrome (NS) in two third of the early onset cases. This study was carried out to assess the frequencies of mutations in these genes in a cohort of pediatric NS patients. A total of 64 pediatric familial o...

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Bibliographic Details
Main Authors: Aiysha Abid, Saba Shahid, Madiha Shakoor, Ali A. Lanewala, Seema Hashmi, Shagufta Khaliq
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-06-01
Series:Frontiers in Genetics
Subjects:
WT1
Online Access:https://www.frontiersin.org/article/10.3389/fgene.2018.00214/full