Fine Mapping Implicates a Deletion of CFHR1 and CFHR3 in Protection from IgA Nephropathy in Han Chinese

An intronic variant at the complement factor H (CFH) gene on chromosome 1q32 (rs6677604) associates with risk of IgA nephropathy (IgAN), but the association signal has not been uniformly replicated in Han Chinese populations. We investigated whether the causal sequence variant resides in the CFH gen...

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Detaylı Bibliyografya
Yayımlandı:J Am Soc Nephrol
Asıl Yazarlar: Xie, Jingyuan, Kiryluk, Krzysztof, Li, Yifu, Mladkova, Nikol, Zhu, Li, Hou, Ping, Ren, Hong, Wang, Weiming, Zhang, Hong, Chen, Nan, Gharavi, Ali G.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society of Nephrology 2016
Konular:
Clinical Research
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5042673/
https://ncbi.nlm.nih.gov/pubmed/26940089
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2015111210
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