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eNauka >  Results >  Mutations in uroplakin IIIA are a rare cause of renal hypodysplasia in humans
Title: Mutations in uroplakin IIIA are a rare cause of renal hypodysplasia in humans
Authors: Schonfelder, EM; Knuppel, T; Tasic, Velibor; Miljkovic, Predrag; Konrad, Martin; Wuhl, E; Antignac, C; Bakkaloglu, A; Schaefer, F; Weber, Stefanie
Issue Date: 2006
Publication: AMERICAN JOURNAL OF KIDNEY DISEASES
ISSN: 0272-6386 American Journal of Kidney Diseases Search Idenfier
Type: Article
Collation: vol. 47 br. 6 str. 1004-1012
DOI: 10.1053/j.ajkd.2006.02.177
WoS-ID: 000238390400008
Scopus-ID: 2-s2.0-33646791894
URI: https://enauka.gov.rs/handle/123456789/799181
Metadata source: (Preuzeto iz Nasi u WoS)
M-category: 
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