Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract

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Naziv:	Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract
Autori :	Zheng, Bixia; ...; Stajic, Natasa; ...; (broj, koautora 17)
Godina:	2021
Publikacija:	NEPHROLOGY DIALYSIS TRANSPLANTATION
ISSN:	0931-0509 Nephrology Dialysis Transplantation Pretraži identifikator
Tip rezultata:	Naučni članak
Kolacija:	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
Projekat:	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
Izvor metapodataka:	(Preuzeto iz Nasi u WoS)
M-kategorija:	21aM21a - Vodeći međunarodni časopis kategorije M21a

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