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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438956/ https://www.ncbi.nlm.nih.gov/pubmed/30967869 http://dx.doi.org/10.3389/fimmu.2019.00537 |