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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Bibliografski detalji
Izdano u:J Am Soc Nephrol
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: American Society of Nephrology 2018
Teme:
Clinical Research
Online pristup: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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