Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy

Benjamin Cogné(Centre National de la Recherche Scientifique), Xénia Latypova(Centre National de la Recherche Scientifique), Lokuliyanage Dona Samudita Senaratne(Oslo University Hospital), Ludovic Martin(Inserm), Daniel C. Koboldt(Nationwide Children's Hospital), Georgios Kellaris(Duke University), Lorraine Fievet(Duke University), Guylène Le Meur(Centre Hospitalier Universitaire de Nantes), D. Caldari(Hôpital Mère-Enfant), Dominique Debray(Hôpital Necker-Enfants Malades), Mathilde Nizon(Centre National de la Recherche Scientifique), Eirik Frengen(Oslo University Hospital), Sara J. Bowne(The University of Texas Health Science Center at Houston), Reuben M. Buckley(The University of Texas Health Science Center at Houston), Danielle Aberdein(The University of Texas Health Science Center at Houston), Paulo C. Alves(Massachusetts Eye and Ear Infirmary), Gregory S. Barsh(Massachusetts Eye and Ear Infirmary), Rebecca R. Bellone(University of California, Los Angeles), Tomas F. Bergström(Northwestern University), Adam R. Boyko(Centre National de la Recherche Scientifique), Jeffrey A. Brockman(Michigan State University), Margret L. Casal(Michigan State University), Marta G. Castelhano(Missouri College), O. Distl(Hôpital Necker-Enfants Malades), Nicholas H. Dodman(The University of Texas Health Science Center at Houston), N. Matthew Ellinwood(Northwestern University), Jonathan E. Fogle(Centre National de la Recherche Scientifique), Oliver P. Forman, Dorian J. Garrick, Edward I. Ginns, Jens Häggström, Robert J. Harvey, Daisuke Hasegawa, Bianca Haase, Chris R. Helps, Isabel Hernández, Marjo K. Hytönen, Maria Kaukonen, Christopher B. Kaelin, Tomoki Kosho, Emilie Leclerc, T.L. Lear, Tosso Leeb, Ronald H. L. Li, Hannes Lohi, M. Longeri, Mark A. Magnuson, Richard Malík, Shrinivasrao P. Mane, John S. Munday, William J. Murphy, Niels C. Pedersen, Max F. Rothschild, Clare Rusbridge, Beth Shapiro, Joshua A. Stern, William F. Swanson, Karen A. Terio(The University of Texas Health Science Center at Houston), Rory J. Todhunter, Wesley C. Warren, Elizabeth A. Wilcox, Julia H Wildschutte, Yoshihiko Yu, Elizabeth L. Cadena(The University of Texas Health Science Center at Houston), Stephen P. Daiger(The University of Texas Health Science Center at Houston), Kinga M. Bujakowska(Massachusetts Eye and Ear Infirmary), Eric A. Pierce(Massachusetts Eye and Ear Infirmary), Michael B. Gorin(University of California, Los Angeles), Nicholas Katsanis(Northwestern University), Stéphane Bezieau(Centre National de la Recherche Scientifique), Simon M. Petersen‐Jones(Michigan State University), Laurence M. Occelli(Michigan State University), Leslie A. Lyons(Missouri College), Laurence Legeai‐Mallet(Hôpital Necker-Enfants Malades), Lori S. Sullivan(The University of Texas Health Science Center at Houston), Erica E. Davis(Lurie Children's Hospital), Bertrand Isidor(Centre National de la Recherche Scientifique)
The American Journal of Human Genetics
May 7, 2020
Cited by 55Open Access
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