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Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract
| Title: | Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract | Authors  : | Zheng, Bixia; ...; Stajic, Natasa; ...; (broj, koautora 17) | Issue Date: | 2021 | Publication: | NEPHROLOGY DIALYSIS TRANSPLANTATION | ISSN: | 0931-0509 Nephrology Dialysis Transplantation Search Idenfier |
Type: | Article | Collation: | vol. 37 br. 10 str. 1833-1843 | DOI: | 10.1093/ndt/gfab253 | WoS-ID: | 000792260800001 | Scopus-ID: | 2-s2.0-85138459100 | PMID: | 34473308 | PMCID: | PMC9755999 | URI: | https://enauka.gov.rs/handle/123456789/825381 | Project: | Begg Family Foundation program of China Scholarships Council [201908320472] Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [442070894] Health Research Board, Ireland [HPF-206-674] International Pediatric Research Foundation Early In |
Metadata source: | (Preuzeto iz Nasi u WoS) | M-category: | 21aM21a |
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