A haplotype in CFH family genes confers high risk of rare glomerular nephropathies

Despite distinct renal lesions, a series of rare glomerular nephropathies are reportedly mediated by complement overactivation. Genetic variations in complement genes contribute to disease risk, but the relationship of genotype to phenotype has not been straightforward. Here, we screened 11 compleme...

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Detalles Bibliográficos
Autores principales: Ding, Yin, Zhao, Weiwei, Zhang, Tao, Qiang, Hao, Lu, Jianping, Su, Xin, Wen, Shuzhen, Xu, Feng, Zhang, Mingchao, Zhang, Haitao, Zeng, Caihong, Liu, Zhihong, Chen, Huimei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519609/
https://www.ncbi.nlm.nih.gov/pubmed/28729648
http://dx.doi.org/10.1038/s41598-017-05173-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519609/
https://www.ncbi.nlm.nih.gov/pubmed/28729648
http://dx.doi.org/10.1038/s41598-017-05173-8

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