Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy (vol 110, pg 120, 2023) Maimuna S. Paul , Anna R. Duncan , Casie A. Genetti , Hongling Pan , Adam Jackson , Patricia E. Grant , Jiahai Shi , Michele Pinelli , Nicola Brunetti-Pierri , Alexandra Garza-Flores , Dave Shahani , Russell P. Saneto , Giuseppe Zampino , Chiara Leoni , Emanuele Agolini , Antonio Novelli , B. Ulrike Blumlein Tobias B. Haack , Wolfram Heinritz , Eva Matzker , Bader Alhaddad , Rami Abou Jamra , Tobias Bartolomaeus , Saber AlHamdan , Raphael Carapito , Bertrand Isidor , Seiamak Bahram , Alyssa Ritter , Kosuke Izumi , Ben Pode Shakked , Ortal Barel , Bruria Ben Zeev , Amber Begtrup , Deanna Alexis Carere , Sureni V. Mullegama , Timothy Blake Palculict , Daniel G. Calame , Katharina Schwan , Alicia R. P. Aycinena , Rasa Traberg , Sofia Douzgou , Harrison Pirt , Naila Ismayilova , Siddharth Banka , Hsiao-Tuan Chao , Pankaj B. Agrawal AMERICAN JOURNAL OF HUMAN GENETICS（2023）
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