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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Sci Rep
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group UK 2017
Aiheet:
Article
Linkit: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
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia