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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Detalles Bibliográficos
Autores principales: Abid, Aiysha, Shahid, Saba, Shakoor, Madiha, Lanewala, Ali A., Hashmi, Seema, Khaliq, Shagufta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036290/
https://www.ncbi.nlm.nih.gov/pubmed/30013592
http://dx.doi.org/10.3389/fgene.2018.00214

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036290/
https://www.ncbi.nlm.nih.gov/pubmed/30013592
http://dx.doi.org/10.3389/fgene.2018.00214

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