Skip to main content
PMC home page
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 2023 Mar 2;110(3):548. doi: 10.1016/j.ajhg.2023.02.010

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy

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, Ulrike Blümlein 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 RP Aycinena, Rasa Traberg; Genomics England Research Consortium, Sofia Douzgou, Harrison Pirt, Naila Ismayilova, Siddharth Banka, Hsiao-Tuan Chao ∗, Pankaj B Agrawal ∗∗
PMCID: PMC10027494  PMID: 36868207

(The American Journal of Human Genetics 110, 120–145; January 5, 2023)

In the originally published version of this article, the stock number of two fly lines, UAS-eIF4A and Nubbin-GAL4, are incorrectly mentioned. The correct stock number for UAS-eIF4A is FlyORF:F000979 and for Nubbin-GAL4 is BDSC #86108. This has now been fixed online. The authors regret this inadvertent error.

Contributor Information

Hsiao-Tuan Chao, Email: hc140077@bcm.edu.

Pankaj B. Agrawal, Email: pankaj.agrawal@enders.tch.harvard.edu.

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES