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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

Genetics in Medicine Open（2024）

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