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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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Detaylı Bibliyografya
Yayımlandı:Front Genet
Asıl Yazarlar: Abid, Aiysha, Shahid, Saba, Shakoor, Madiha, Lanewala, Ali A., Hashmi, Seema, Khaliq, Shagufta
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2018
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6036290/
https://ncbi.nlm.nih.gov/pubmed/30013592
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2018.00214
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