Genetics in Medicine Open (Jan 2024)
O07: Haploinsufficiency of EIF3A and EIF3B cause a clinically variable phenotype characterized by neurodevelopmental abnormalities and congenital heart defects
- Cherith Somerville,
- Ersa Erkut,
- Marci Schwartz,
- Xin Chen,
- Roozbeh Manshaei,
- Qiliang Ding,
- Karin Diderich,
- Lisa Herzig,
- Bri Dingmann,
- Chloe Quelin,
- Véronique Pingault,
- Christèle Dubourg,
- Joana Rosmaninho Salgado,
- Sérgio Sousa,
- Daniel Koboldt,
- Rachel Gosselin,
- Kim McBride,
- Maria Arvio,
- Irma Järvelä,
- Isabelle Schrauwen,
- Laura Conlin,
- Cara Skraban,
- Sara Reichert,
- Jacqueline Leonard,
- Emma Bedoukian,
- Raymond Kim,
- Ian Scott,
- Rebekah Jobling
Affiliations
- Cherith Somerville
- Ted Rogers Centre for Heart Research, Cardiac Genome Clinic, The Hospital for Sick Children, Toronto, Ontario, Canada
- Ersa Erkut
- Program in Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada
- Marci Schwartz
- Ted Rogers Centre for Heart Research, Cardiac Genome Clinic, The Hospital for Sick Children, Toronto, Ontario, Canada
- Xin Chen
- Ted Rogers Centre for Heart Research, Cardiac Genome Clinic, The Hospital for Sick Children, Toronto, Ontario, Canada
- Roozbeh Manshaei
- Ted Rogers Centre for Heart Research, Cardiac Genome Clinic, The Hospital for Sick Children, Toronto, Ontario, Canada
- Qiliang Ding
- Ted Rogers Centre for Heart Research, Cardiac Genome Clinic, The Hospital for Sick Children, Toronto, Ontario, Canada
- Karin Diderich
- Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands
- Lisa Herzig
- Seattle Children's Hospital, University of Washington, Seattle, WA
- Bri Dingmann
- Seattle Children's Hospital, University of Washington, Seattle, WA
- Chloe Quelin
- Service de Génétique Clinique, CLAD Ouest, CHU Rennes, Rennes, France
- Véronique Pingault
- Service de Médecine Génomique des Maladies Rares, AP-HP, Hôpital Necker, Paris, France
- Christèle Dubourg
- Service de Génétique Moléculaire et Génomique, CHU Pontchaillou, Rennes, France
- Joana Rosmaninho Salgado
- Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal
- Sérgio Sousa
- Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal
- Daniel Koboldt
- The Steve and Cindy Rasmussen Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, The Department of Pediatrics at The Ohio State University College of Medicine, Columbus, OH
- Rachel Gosselin
- Division of Genetic and Genomic Medicine at Nationwide Children's Hospital, Columbus, OH
- Kim McBride
- The Department of Pediatrics at The Ohio State University College of Medicine, Columbus, OH, Division of Genetic and Genomic Medicine at Nationwide Children's Hospital, Columbus, OH, Center for Cardiovascular Research at Nationwide Children's Hospital, Columbus, OH, The Department of Medical Genetics, Cumming School of Medicine University of Calgary, Alberta, Canada
- Maria Arvio
- Päijät-Häme Joint Municipal Authority, Neurology, Lahti, Finland; PEDEGO, Oulu University Hospital, Finland, Department of General Practise, Turku University and Turku University Central Hospital, Finland
- Irma Järvelä
- The Department of Medical Genetics, University of Helsinki, Helsinki, Finland
- Isabelle Schrauwen
- Center for Statistical Genetics, Gertrude H. Sergievsky Center, and the Department of Neurology, Columbia University Medical Center, New York, NY
- Laura Conlin
- Children’s Hospital of Philadelphia, Philadelphia, PA
- Cara Skraban
- Children’s Hospital of Philadelphia, Philadelphia, PA
- Sara Reichert
- Children’s Hospital of Philadelphia, Philadelphia, PA
- Jacqueline Leonard
- Children’s Hospital of Philadelphia, Philadelphia, PA
- Emma Bedoukian
- Children’s Hospital of Philadelphia, Philadelphia, PA
- Raymond Kim
- Ted Rogers Centre for Heart Research, Cardiac Genome Clinic, The Hospital for Sick Children, Toronto, Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada, Fred A. Litwin Family Centre in Genetic Medicine, University Health Network, Department of Medicine, University of Toronto, Toronto, Ontario, Canada
- Ian Scott
- Program in Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada, Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada
- Rebekah Jobling
- Ted Rogers Centre for Heart Research, Cardiac Genome Clinic, The Hospital for Sick Children, Toronto, Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada, Genome Diagnostics, Department of Pediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada
- Journal volume & issue
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Vol. 2
p. 101469