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

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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
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Saisawat, P., Kohl, R. H. G., Hilger, A. C., Hwang, D.-Y., Yung Gee, H., Dworschak, G. C., Tasic, V., Pennimpede, T., Natarajan, S., Sperry, E., Matassa, D. S., Stajic, N., Bogdanovic, R., de Blaauw, I., Marcelis, C., Wijers, C., Bartels, E., Schmiedeke, E., Schmidt, D., … Hildebrandt, F. (2013). Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association. Kidney International.https://doi.org/10.1038/ki.2013.417

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