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eNauka >  Results >  Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations
Title: Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations
Authors: Hoskins, Bethan E.; Cramer, Carl H.; Tasić, Velibor; Kehinde, Elijah O.; Ashraf, Shazia; Bogdanović, Radovan; Hoefele, Julia; Pohl, Martin; Hildebrandt, Friedhelm
Issue Date: 2008
Publication: Nephrology, dialysis, transplantation
ISSN: 0931-0509 Nephrology Dialysis Transplantation Search Idenfier
Publisher: London : Springer InternationalOxford : Oxford University Press
Type: Other
Collation: vol. 23 br. 2 str. 777-779
DOI: 10.1093/ndt/gfm685
WoS-ID: 000253022300064
Scopus-ID: 2-s2.0-44449157662
VBS COBISS: 1025594549
URI: https://plus.cobiss.net/cobiss/sr/sr/bib/1025594549#izum.si
https://enauka.gov.rs/handle/123456789/668543
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