Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome.

Journal: American Journal of Human Genetics

Published: 2020-11-05

DOI: 10.1016/j.ajhg.2020.09.005

Affiliations: 28

Authors: 42

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Institutions Share
National Research Centre (NRC), Egypt 0.14
UC San Diego Health Sciences, United States of America (USA) 0.08
University of Antwerp (UA), Belgium 0.08
University of Kassel, Germany 0.07
IRCCS Casa Sollievo della Sofferenza Hospital, Italy 0.07
Odense University Hospital (OUH), Denmark 0.07
Epilepsy Research Centre, Australia 0.06
Institute of Biomedical Research Alberto Sols (IIBM), Spain 0.06
Biomedical Research Networking Center on Rare Diseases (CIBERER), Spain 0.06
University of Oslo (UiO), Norway 0.05
Hospital La Paz Institute for Health Research (IdiPAZ), Spain 0.03
Murdoch Children's Research Institute (MCRI), Australia 0.03
The University of Melbourne (UniMelb), Australia 0.02
Imagine Institute, France 0.02
Centre Hospitalier Universitaire d'Angers (CHU d'Angers), France 0.02
Hôpital Necker-Enfants Malades, France 0.02
MITOVASC, France 0.02
Walter and Eliza Hall Institute of Medical Research (WEHI), Australia 0.02
University of Tasmania (UTAS), Australia 0.02
Antwerp University Hospital (UZA), UA, Belgium 0.01
University of California, San Diego (UC San Diego), United States of America (USA) 0.01
Austin Health, Australia 0.01
Florey Institute of Neuroscience and Mental Health, Australia 0
The Royal Children's Hospital Melbourne (RCH), Australia 0