Characterization of Coding/Noncoding Variants for SHROOM3 in Patients with CKD

Background Interpreting genetic variants is one of the greatest challenges impeding analysis of rapidly increasing volumes of genomic data from patients. For example, SHROOM3 is an associated risk gene for CKD, yet causative mechanism(s) of SHROOM3 allele(s) are unknown. Methods We used our analytic...

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Detalhes bibliográficos
Publicado no:J Am Soc Nephrol
Main Authors: Prokop, Jeremy W., Yeo, Nan Cher, Ottmann, Christian, Chhetri, Surya B., Florus, Kacie L., Ross, Emily J., Sosonkina, Nadiya, Link, Brian A., Freedman, Barry I., Coppola, Candice J., McDermott-Roe, Chris, Leysen, Seppe, Milroy, Lech-Gustav, Meijer, Femke A., Geurts, Aron M., Rauscher, Frank J., Ramaker, Ryne, Flister, Michael J., Jacob, Howard J., Mendenhall, Eric M., Lazar, Jozef
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2018
Assuntos:
Clinical Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5967772/
https://ncbi.nlm.nih.gov/pubmed/29476007
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2017080856
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