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P. Saisawat (Pawaree), R.H.G. Kohl, A.C. Hilger (Alina C), D.-Y. Hwang (Daw-Yang), H. Yung Gee (Heon), G.C. Dworschak (Gabriel C), V. Tasic (Velibor), T. Pennimpede (Tracie), S. Natarajan (Sivakumar), E. Sperry (Ethan), et al. D.S. Matassa (Danilo S), N. Stajic (Natasa), R. Bogdanovic (Radovan), I. de Blaauw (Ivo), C.L.M. Marcelis (Carlo), C.H.W. Wijers (Charlotte), E. Bartels (Enrika), E. Schmiedeke (Eberhard), D. Schmidt (Dedan), S. Märzheuser (Stefanie), S. Grasshoff-Derr (Sabine), S. Holland-Cunz (Stefan), M. Ludwig (Michael), M.M. Nöthen (Markus), M. Draaken (Markus), E. Brosens (Erwin), H.A. Heij (Hugo Anne), D. Tibboel (Dick), B.G. Herrmann (Bernhard G), B.D. Solomon (Benjamin D), J.E.M.M. de Klein (Annelies), I.A.L.M. Rooij (Iris), F. Esposito (Francesco), H. Reutter (Heiko) and F. Hildebrandt (Friedhelm)

2013-10-23

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association

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Kidney International

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Persistent URL doi.org/10.1038/ki.2013.417, hdl.handle.net/1765/55715
Journal Kidney International
Organisation Department of Pediatric Surgery
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Saisawat, P., Kohl, R. H. G., Hilger, A. C., Hwang, D.-Y., Yung Gee, H., Dworschak, G. C., … Hildebrandt, F. (2013). Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association. Kidney International. doi:10.1038/ki.2013.417
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