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DOAJ
Article . 2020
Data sources: DOAJ
Claim

Three cases of steroid resistant nephrotic syndrome associated with gene mutation of transient receptor potential cation channel 6(TRPC 6)in children

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 2020 Chinese Publisher:Editorial Department of Journal of Clinical Nephrology
Authors: SHI Zhuo; GAO Chun-lin; XIA Zheng-kun; SUN Tao; ZHANG Pei;

Three cases of steroid resistant nephrotic syndrome associated with gene mutation of transient receptor potential cation channel 6(TRPC 6)in children

Abstract

原发性肾病综合征中大约有20%的患儿出现激素耐药,其中局灶节段硬化(focal segmental glomerulosclerosis,FSGS)是其主要的病理改变,且多发生于6岁前,并在10岁内进展为ESRD[1-2]。目前已明确多种基因的突变参与FSGS的形成,尤其是编码足细胞相关蛋白的单基因突变在其中发挥重要作用[3]。

Keywords

TRPC 6, Steroid resistant nephrotic syndrome, Gene mutation, Children, Internal medicine, RC31-1245

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
Average
Average
Average
bronze