Work

Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)

Year: 2008

Type: article

Study design: Observational Study

Source: Pediatric Nephrology

DOI: 10.1007/s00467-008-1016-6

Authors: Matthias T. F. Wolf, Bethan E. Hoskins, Bodo B. Beck, Bernd Hoppe, Velibor Tasic, Edgar A. Otto, Friedhelm Hildebrandt

Institutions: University of Michigan, University of Cologne, Ss. Cyril and Methodius University in Skopje

Language: English

Topic: Pediatric Urology and Nephrology Studies

Subfield: Pediatrics, Perinatology and Child Health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: green

Funders: Deutsche Forschungsgemeinschaft, Universität zu Köln, National Institutes of Health, Medical School, University of Michigan, National Institute of Diabetes and Digestive and Kidney Diseases

Awards: Function of NPHP6 a novel gene for Senior-Loken syndrome, G229581314, Functional characterization of the gene NPHP4, G3713441098, G3716821922, Novel genetics, pathobiology and therapy of nephronophthisis-related ciliopathies

OpenAlex ID: W1989137257

FWCI: 2.104

Cites: 25

Cited by: 18

Related to: 10