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...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en: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: American Society of Nephrology 2018
Assuntos:
Clinical Research
Acceso en liña: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
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares