Sequencing rare and common APOL1 coding variants to determine kidney disease risk

A third of African Americans with sporadic focal segmental glomerulosclerosis (FSGS) or HIV-associated nephropathy (HIVAN) do not carry APOL1 renal risk genotypes. This raises the possibility that other APOL1 variants may contribute to kidney disease. To address this question, we sequenced all APOL1...

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Detalhes bibliográficos
Publicado no:Kidney Int
Main Authors: Limou, Sophie, Nelson, George W, Lecordier, Laurence, An, Ping, O’hUigin, Colm S, David, Victor A, Binns-Roemer, Elizabeth A, Guiblet, Wilfried M, Oleksyk, Taras K, Pays, Etienne, Kopp, Jeffrey B, Winkler, Cheryl A
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4591109/
https://ncbi.nlm.nih.gov/pubmed/25993319
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ki.2015.151
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