De Novo Variants in MAPK8IP3 Cause Intellectual Disability with Variable Brain Anomalies.

Journal: American Journal of Human Genetics

Published: 2018-12-31

DOI: 10.1016/j.ajhg.2018.12.008

Affiliations: 25

Authors: 32

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Institutions FC
Institute of Human Genetics, Leipzig University, Germany 0.09
Levine Children's Hospital, Atrium Health, United States of America (USA) 0.06
GeneDx, United States of America (USA) 0.06
Mendelics Genomic Analysis, Brazil 0.06
Fullerton Genetics Center, Mission Health, United States of America (USA) 0.06
OMRF Genetic Models of Disease Laboratory, United States of America (USA) 0.06
Institute of Human Genetics, GMC, Israel 0.05
Department of Pediatrics, CU Anschutz, United States of America (USA) 0.03
CeGaT GmbH, Germany 0.03
Institute for Clinical Genetics, TU Dresden, Germany 0.03
School for Oncology and Developmental Biology (GROW), Maastricht UMC+, Netherlands 0.03
Department of Clinical Genetics, Maastricht UMC+, Netherlands 0.03
Ambry Genetics, United States of America (USA) 0.03
Department of Pediatrics, SLU, United States of America (USA) 0.03
Praxis für Humangenetik Tübingen, Germany 0.03
Johns Hopkins University School of Medicine (JHUSOM), JHU, United States of America (USA) 0.03
Kindergeneeskunde, Zuyderland Medisch Centrum, Netherlands 0.03
Department of Paediatrics and Adolescent Medicine, WWU, Germany 0.03
IRCCS Italian Institute for Auxology, Italy 0.03
Neurology and Neurogenetics Clinic, Kennedy Krieger Institute, United States of America (USA) 0.03
Institute of Biochemistry, FAU, Germany 0.03
Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII (ASST-PG23), Italy 0.03
Institute of Human Genetics, UKSH Lübeck, Germany 0.03
Department of Pediatrics, UT Health, United States of America (USA) 0.03
Faculty of Medicine, BIU, Israel 0.02

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