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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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5519609/
https://ncbi.nlm.nih.gov/pubmed/28729648
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-05173-8
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