Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/28733
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dc.contributor.authorVu, Thi Thom-
dc.contributor.authorPham, Van Dem-
dc.contributor.authorVu, Van Nga-
dc.contributor.authorPham, Thi Hong Nhung-
dc.contributor.authorNguyên, Thi Quynh Huong-
dc.contributor.authorDoan, Dinh Long-
dc.date.accessioned2020-07-16T00:46:08Z-
dc.date.available2020-07-16T00:46:08Z-
dc.date.issued2019-
dc.identifier.issn1811-4989-
dc.identifier.urihttp://dspace.ctu.edu.vn/jspui/handle/123456789/28733-
dc.description.abstractNephrotic syndrome in children is traditionally classified according to the standard steroid treatment response, and in Vietnamese children about 12.4% of cases are steroid resistant. Currently, more than 24 genes have been associated with nephrotic syndrome in children, with three, NPHS1, NPHS2 and WT1, having a major impact on steroid resistant nephrotic syndrome. This study aims to investigate NPHS2 variants in different nephrotic syndrome groups defined as steroid sensitive nephrotic syndrome (SSNS), steroid resistant nephrotic syndrome (SRNS).vi_VN
dc.language.isoenvi_VN
dc.relation.ispartofseriesJournal of Biotechnology;No 17(02) .- Page.231-237-
dc.subjectNPHS2vi_VN
dc.subjectPediatric nephrotic syndrome patientsvi_VN
dc.subjectSterotd-resistant nephrotic syndromevi_VN
dc.subjectSteroid-sensitive nephrotic syndromevi_VN
dc.titleRole of NPHS2 gene variants IN steroid response and edema level of Vietnamese pediatric patients with primary nephrotic syndromevi_VN
dc.typeArticlevi_VN
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