A Rare Genetic Defect of MBL2 Increased the Risk for Progression of IgA Nephropathy

The aim of this study was to investigate the association between lectin pathway-related genetic variations and progression in IgA nephropathy. Biopsy-proven IgAN patients with eGFR ≥15 ml/min/1.73 m(2) at baseline and a minimum follow-up of 12-months were enrolled. A total of 1,007 patients and 121...

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Dades bibliogràfiques
Publicat a:Front Immunol
Autors principals: Ouyang, Yan, Zhu, Li, Shi, Manman, Yu, Shuwen, Jin, Yuanmeng, Wang, Zhaohui, Ma, Jun, Yang, Meng, Zhang, Xiaoyan, Pan, Xiaoxia, Ren, Hong, Wang, Weiming, Zhang, Hong, Xie, Jingyuan, Chen, Nan
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2019
Matèries:
Immunology
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6438956/
https://ncbi.nlm.nih.gov/pubmed/30967869
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2019.00537
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