Recurrent Dominant Mutations Affecting Two Adjacent Residues in the Motor Domain of the Monomeric Kinesin KIF22 Result in Skeletal Dysplasia and Joint Laxity
Eric D. Boyden(Howard Hughes Medical Institute), Luisa Bonafé(University of Lausanne), Richard H. Scott(Genomics England), Belinda Campos‐Xavier(University of Lausanne), Trevor L. Cameron(Murdoch Children's Research Institute), Andrea Superti‐Furga(University of Lausanne), John F. Bateman(The University of Melbourne), André Mégarbané(University Medical Center Groningen), Geert Mortier(Center for Human Genetics), Massimiliano Rossi(Hospices Civils de Lyon), Gen Nishimura(Musashino University), Generoso Andria(Federico II University Hospital), Goranka Tanackovich(University of Lausanne), Philippe Suarez(University of Lausanne), Matthew L. Warman(Boston Children's Hospital), Sebastian Kalamajski(Lund University), Pierre‐Simon Jouk, Sheila Unger(University of Lausanne), Michael D. Briggs(Centre for Life), Rainer König(Jena University Hospital), Daniel H. Cohn(University of California, Los Angeles), H. Rosemarie Davidson(Woolmanhill Hospital), Eugênia Ribeiro Valadares(Universidade Federal de Minas Gerais), Hirotake Sawada(University of Miyazaki Hospital), Christine M Hall(Great Ormond Street Hospital), Claire Hartley(Wellcome Centre for Cell-Matrix Research), Ralph S. Lachman(Cedars-Sinai Medical Center), R. Curtis Rogers(Greenwood Genetic Center), Diana Ballhausen(University of Lausanne), David L. Rimoin(Los Angeles City College), Shiro Ikegawa(RIKEN Center for Integrative Medical Sciences)
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