SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1–SIX1–DNA complexes
Rainer Ruf(Martin-Luther-Krankenhaus), Friedhelm Hildebrandt(Boston Children's Hospital), Richard J. Smith(University of Iowa), Shrawan Kumar(Boys Town), Derek Silvius(Boys Town), Ulla Muerb(Boys Town), Constantine A. Stratakis(Institute of Molecular Biology and Biotechnology), Jennifer Berkman(Boys Town), Eugene H. Chang(University of Arizona), V.J. Hyland(Boys Town), Edgar A. Otto(University of Michigan), Pin‐Xian Xu(Brigham and Women's Hospital), Michael Gattas(Boys Town), Dominique Weil(Boys Town), Christine Petit(Inserm), Charles E. Schwartz(Greenwood Genetic Center), Patrick D. Brophy, Frank Beekmann(University of Michigan–Ann Arbor), Markus J. Kemper(University of Zurich), Eva-Maria Ruf(Boys Town), Thomas J. Neuhaus(University of Zurich), Richard M. Raymond(Boys Town)
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