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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Vydáno v:Front Genet
Hlavní autoři: Abid, Aiysha, Shahid, Saba, Shakoor, Madiha, Lanewala, Ali A., Hashmi, Seema, Khaliq, Shagufta
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2018
Témata:
Genetics
On-line přístup: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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