Exome-Based Rare-Variant Analyses in CKD

BACKGROUND: Studies have identified many common genetic associations that influence renal function and all-cause CKD, but these explain only a small fraction of variance in these traits. The contribution of rare variants has not been systematically examined. METHODS: We performed exome sequencing of...

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Detalhes bibliográficos
Publicado no:J Am Soc Nephrol
Main Authors: Cameron-Christie, Sophia, Wolock, Charles J., Groopman, Emily, Petrovski, Slavé, Kamalakaran, Sitharthan, Povysil, Gundula, Vitsios, Dimitrios, Zhang, Mengqi, Fleckner, Jan, March, Ruth E., Gelfman, Sahar, Marasa, Maddalena, Li, Yifu, Sanna-Cherchi, Simone, Kiryluk, Krzysztof, Allen, Andrew S., Fellström, Bengt C., Haefliger, Carolina, Platt, Adam, Goldstein, David B., Gharavi, Ali G.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2019
Assuntos:
Clinical Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6551770/
https://ncbi.nlm.nih.gov/pubmed/31085678
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2018090909
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