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Genome-wide scan identifies a copy number variable region at 3p21.1 that influences the TLR9 expression levels in IgA nephropathy patients

Immunoglobulin A nephropathy (IgAN) is a complex multifactorial disease characterized by genetic factors that influence the pathogenesis of the disease. In this context, an intriguing role could be ascribed to copy number variants (CNVs). We performed the whole-genome screening of CNVs in familial I...

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Detaylı Bibliyografya
Yayımlandı:Eur J Hum Genet
Asıl Yazarlar: Sallustio, Fabio, Cox, Sharon N, Serino, Grazia, Curci, Claudia, Pesce, Francesco, De Palma, Giuseppe, Papagianni, Aikaterini, Kirmizis, Dimitrios, Falchi, Mario, Schena, Francesco P
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group 2015
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4463498/
https://ncbi.nlm.nih.gov/pubmed/25293716
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2014.208
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