Erratum: Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy (The American Journal of Human Genetics (2023) 110(1) (120–145), (S000292972200502X), (10.1016/j.ajhg.2022.11.011))

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 R.P. Aycinena; Rasa Traberg; Sofia Douzgou; Harrison Pirt; Naila Ismayilova; Siddharth Banka; Hsiao Tuan Chao; Pankaj B. Agrawal

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Erratum: Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy (The American Journal of Human Genetics (2023) 110(1) (120–145), (S000292972200502X), (10.1016/j.ajhg.2022.11.011))

American Journal of Human Genetics

DOI: 10.1016/j.ajhg.2023.02.010

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Abstract

(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.

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Paul, M. S., Duncan, A. R., Genetti, C. A., Pan, H., Jackson, A., Grant, P. E., … Agrawal, P. B. (2023, March 2). Erratum: Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy (The American Journal of Human Genetics (2023) 110(1) (120–145), (S000292972200502X), (10.1016/j.ajhg.2022.11.011)). American Journal of Human Genetics. Cell Press. https://doi.org/10.1016/j.ajhg.2023.02.010

Erratum: Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy (The American Journal of Human Genetics (2023) 110(1) (120–145), (S000292972200502X), (10.1016/j.ajhg.2022.11.011))

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