Analysis of NPHS2 Gene Mutations in Egyptian Children with Nephrotic Syndrome

BACKGROUND: Mutations in the NPHS2 genes are the main aetiology of early-onset and familial steroid-resistant nephrotic syndrome (SRNS). The pathogenic NPHS2 mutation together with the p.R229Q variant has been less described among Egyptian children. AIM: This study aims to determine the mutation of...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Open Access Maced J Med Sci
Prif Awduron: Zaki, Moushira, El-Shaer, Shreen, Rady, Sahar, El-Salam, Manal Abd, Abd-El-Salam, Ragaa, Alkashlan, Ibrahim Abdelfattah, Saber, Mohamed, Mohamed, Sanaa, Hassaan, Mohamed, Rabie, Eman, Amr, Khalda
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Republic of Macedonia 2019
Pynciau:
Basic Science
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6953933/
https://ncbi.nlm.nih.gov/pubmed/31949506
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3889/oamjms.2019.700
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