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

Journal: American Journal of Human Genetics

Published: 2020-04-28

DOI: 10.1016/j.ajhg.2020.04.005

Affiliations: 19

Authors: 27

Go to article
Institutions Share
Human Genetics Center (HGC), UTHealth, United States of America (USA) 0.13
Service de Génétique Médicale, CHU de Nantes, France 0.12
Duke Center for Human Disease Modeling (CHDM), United States of America (USA) 0.10
Institut du Thorax (IdT), France 0.09
Oslo University Hospital (OUS), Norway 0.07
Ocular Genomics Institute, MEEI, United States of America (USA) 0.07
Department of Small Animal Clinical Sciences (SCS), MSU, United States of America (USA) 0.07
Imagine Institute, France 0.06
Institute for Genomic Medicine (IGM), Nationwide Children’s Hospital, United States of America (USA) 0.04
University Hospital Nantes (CHU de Nantes), France 0.04
Centre de Référence des Surdités Génétiques, Hôpital Necker-Enfants Malades, France 0.04
UCLA Jules Stein Eye Institute (JSEI), United States of America (USA) 0.04
Department of Veterinary Medicine and Surgery (VMS), Mizzou, United States of America (USA) 0.04
Department of Ophthalmology and Visual Science, UTHealth, United States of America (USA) 0.02
Stanley Manne Children’s Research Institute, NU, United States of America (USA) 0.02
Department of Pediatrics, NU, United States of America (USA) 0.02
Hôpital Necker-Enfants Malades, France 0.02
Advanced Center for Translational and Genetic Medicine (ACT-GeM), NU, United States of America (USA) 0.02

Return