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CUBN variants uncouple proteinuria from kidney function.
Nature Reviews Nephrology ( IF 41.5 ) Pub Date : 2019-12-13 , DOI: 10.1038/s41581-019-0242-4
Catherine Quinlan 1, 2, 3
Affiliation  

A new study links pathogenic cubilin gene (CUBN) variants to proteinuria without progressive renal impairment, providing reassurance for a subset of patients, calling into question the accepted pathogenesis of glomerulosclerosis and suggesting future therapeutic options.

中文翻译:

CUBN变体使蛋白尿与肾脏功能脱钩。

一项新研究将致病性cubicin基因(CUBN)变体与蛋白尿相关联,而无进行性肾功能不全,为部分患者提供了保证,质疑肾小球硬化的公认发病机制,并提出了未来的治疗选择。
更新日期:2019-12-13
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