Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations

Bethan E. Hoskins; Carl H. Cramer; Velibor Tasic; Elijah O. Kehinde; Shazia Ashraf; Radovan Bogdanovic; Julia Hoefele; Martin Pohl; Friedhelm Hildebrandt

doi:10.1093/ndt/gfm685

Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations

Bethan E. Hoskins, Carl H. Cramer, Velibor Tasic, Elijah O. Kehinde, Shazia Ashraf, Radovan Bogdanovic, Julia Hoefele, Martin Pohl, Friedhelm Hildebrandt

Department of Medicine

Research output: Contribution to journal › Letter › peer-review

18 Citations (Scopus)

Original language	English
Pages (from-to)	777-779
Number of pages	3
Journal	Nephrology Dialysis Transplantation
Volume	23
Issue number	2
DOIs	https://doi.org/10.1093/ndt/gfm685
Publication status	Published - Feb 1 2008

ASJC Scopus subject areas

Nephrology
Transplantation

Access to Document

10.1093/ndt/gfm685

Cite this

Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations. / Hoskins, Bethan E.; Cramer, Carl H.; Tasic, Velibor; Kehinde, Elijah O.; Ashraf, Shazia; Bogdanovic, Radovan; Hoefele, Julia; Pohl, Martin; Hildebrandt, Friedhelm.

In: Nephrology Dialysis Transplantation, Vol. 23, No. 2, 01.02.2008, p. 777-779.

Research output: Contribution to journal › Letter › peer-review

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