Heterozygous iRAB3A/i variants cause cerebellar ataxia by a partial loss-of-function mechanism

Journal:
Brain
Published:
DOI:
10.1093/brain/awaf111
Affiliations:
31
Authors:
35
Institutions Authors Share
University of Tübingen (Uni Tübingen), Germany
7.166667
0.20
DZNE Site Tübingen, Germany
4.833333
0.14
NIH National Human Genome Research Institute (NHGRI), United States of America (USA)
2.000000
0.06
Essen University Hospital, Germany
2.000000
0.06
McGill University, Canada
1.833333
0.05
University of Miami (UM), United States of America (USA)
1.333333
0.04
University of Bristol (UoB), United Kingdom (UK)
1.000000
0.03
Birmingham Women's Hospital, Birmingham Women's and Children's NHS Foundation Trust, United Kingdom (UK)
1.000000
0.03
Nuffield Orthopaedic Centre NHS Trust, United Kingdom (UK)
1.000000
0.03
Albany Medical Center, United States of America (USA)
1.000000
0.03
Boston Children's Hospital (BCH), United States of America (USA)
1.000000
0.03
Dijon University Hospital, France
1.000000
0.03
Antwerp University Hospital (UZA), UA, Belgium
1.000000
0.03
University of Antwerp (UA), Belgium
1.000000
0.03
University of Alberta (U of A), Canada
1.000000
0.03
University of Maryland, Baltimore (UMB), United States of America (USA)
1.000000
0.03
Center for Interdisciplinary Research in Biology (CIRB), France
1.000000
0.03
Icahn School of Medicine at Mount Sinai (ISMMS), MSHS, United States of America (USA)
1.000000
0.03
University of Massachusetts Chan Medical School (UMass Chan Medical School), United States of America (USA)
1.000000
0.03
Montreal Neurological Institute and Hospital (MNI), McGill University, Canada
0.666667
0.02
Genetics of Development Disorders Team (GAD), France
0.500000
0.01
Fédération Hospitalo-Universitaire Médecine TRANSLationnelle et Anomalies du Développement (FHU-TRANSLAD), France
0.500000
0.01
Broad Institute of MIT and Harvard, United States of America (USA)
0.500000
0.01
Centogene AG, Germany
0.333333
0.01
University Medicine Rostock, Germany
0.333333
0.01