SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling.

Journal: American Journal of Human Genetics

Published: 2020-12-07

DOI: 10.1016/j.ajhg.2020.11.015

Affiliations: 33

Authors: 46

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Institutions Share
IRCCS Bambino Gesù Children's Hospital, Italy 0.24
Hospital das Clínicas da FMUSP, Brazil 0.07
Centogene AG, Germany 0.07
University of Würzburg (JMU), Germany 0.05
Johns Hopkins Aramco Healthcare Company (JHAH), Saudi Arabia 0.04
Kasturba Medical College (KMC), MAHE, India 0.04
Gaziantep Children's Hospital, Turkey 0.04
Abu Dhabi Health Services Company (SEHA), United Arab Emirates 0.04
Leiden University Medical Center (LUMC), Netherlands 0.04
NIHR Oxford Biomedical Research Centre (OxBRC), United Kingdom (UK) 0.04
Rambam Health Care Campus (RambamHCC), IIT, Israel 0.03
King Faisal Specialist Hospital and Research Centre (KFSH&RC), Saudi Arabia 0.03
Guy's Hospital, Guy's and St Thomas' NHS Foundation Trust, United Kingdom (UK) 0.03
University of Isfahan (UI), Iran 0.02
Amsterdam UMC, Netherlands 0.02
St George's, University of London (SGUL), United Kingdom (UK) 0.02
Wohl Institute for Translational Medical Research - Chaim Sheba Site, Israel 0.02
Institute of Biomedical Sciences (IBMS), Academia Sinica, Taiwan 0.02
Taipei Medical University (TMU), Taiwan 0.02
Edmond and Lily Safra Children's Hospital, Chaim Sheba Medical Center, Israel 0.02
Tel Aviv University (TAU), Israel 0.02
Chaim Sheba Medical Center at Tel HaShomer, Israel 0.01
University Hospital Tübingen (UKT), Uni Tübingen, Germany 0.01
Qatar Biomedical Research Institute (QBRI), HBKU, Qatar 0.01
Technion-Israel Institute of Technology (IIT), Israel 0.01
National Yang Ming Chiao Tung University (NYCU), Taiwan 0.01
Birmingham Women's and Children's NHS Foundation Trust, United Kingdom (UK) 0.01
University of Birmingham (UB), United Kingdom (UK) 0.01