Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities

Journal:
American Journal of Human Genetics
Published:
DOI:
10.1016/j.ajhg.2021.04.004
Affiliations:
28
Authors:
41
Institutions Authors Share
Imaging and Brain, France
6.000000
0.15
University Hospital in Motol, Czech Republic
3.000000
0.07
Centre Hospitalier Régional Universitaire de TOURS (CHRU de Tours), France
3.000000
0.07
Institut du Thorax (IdT), France
2.500000
0.06
MITOVASC, France
2.000000
0.05
The University of Arizona (Arizona), United States of America (USA)
2.000000
0.05
Amsterdam UMC, Netherlands
2.000000
0.05
Erasmus University Medical Center (Erasmus MC), Netherlands
2.000000
0.05
Yerevan Mkhitar Heratsi State Medical University (YSMU), Armenia
2.000000
0.05
University of California, San Francisco (UCSF), United States of America (USA)
2.000000
0.05
Birmingham Women's Hospital, Birmingham Women's and Children's NHS Foundation Trust, United Kingdom (UK)
1.500000
0.04
Birmingham Health Partners (BHP), United Kingdom (UK)
1.500000
0.04
Seattle Children's Research Institute, United States of America (USA)
1.500000
0.04
University Hospital Nantes (CHU de Nantes), France
1.500000
0.04
CHRU Brest, France
1.000000
0.02
Broad Institute of MIT and Harvard, United States of America (USA)
1.000000
0.02
Akron Children's Hospital, United States of America (USA)
1.000000
0.02
Karolinska Institute (KI), Sweden
1.000000
0.02
Lipids, Nutrition, Cancer (LNC), France
0.500000
0.01
Dijon University Hospital, France
0.500000
0.01
CHU de Poitiers, France
0.500000
0.01
University of Poitiers, France
0.500000
0.01
Rennes University Hospital (CHU Rennes), France
0.500000
0.01
Institute of Genetics and Development of Rennes (IGDR), France
0.500000
0.01
University of Washington (UW), United States of America (USA)
0.500000
0.01
Institut NeuroMyoGène (INMG), France
0.500000
0.01
Lyon University Hospital (HCL), France
0.500000
0.01