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))

Genomics England Research Consortium; CA Genetti; M Pinelli; N Brunetti-Pierri; A Garza-Flores; Adam Jackson; D Shahani; RP Saneto; G Zampino; C Leoni; E Agolini; A Novelli; BUBTB Haack; W Heinritz; E Matzker; B Alhaddad; R Abou Jamra; T Bartolomaeus; S AlHamdan; R Carapito; B Isidor; S Bahram; A Ritter; K Izumi; B Shakked; O Barel; B Ben Zeev; A Begtrup; DA Carere; SV Mullegama; TB Palculict; DG Calame; K Schwan; ARP Aycinena; R Traberg; S Douzgou; H Pirt; S Banka; HT Chao

doi: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))

Genomics England Research Consortium, CA Genetti, M Pinelli, N Brunetti-Pierri, A Garza-Flores, Adam Jackson, D Shahani, RP Saneto, G Zampino, C Leoni, E Agolini, A Novelli, BUBTB Haack, W Heinritz, E Matzker, B Alhaddad, R Abou Jamra, T Bartolomaeus, S AlHamdan, R CarapitoB Isidor, S Bahram, A Ritter, K Izumi, B Shakked, O Barel, B Ben Zeev, A Begtrup, DA Carere, SV Mullegama, TB Palculict, DG Calame, K Schwan, ARP Aycinena, R Traberg, S Douzgou, H Pirt, S Banka, HT Chao

Division of Evolution, Infection and Genomics

Research output: Contribution to journal › Commentary/debate › peer-review

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.

Original language	English
Pages (from-to)	548
Number of pages	1
Journal	American Journal of Human Genetics
Volume	110
Issue number	3
DOIs	https://doi.org/10.1016/j.ajhg.2023.02.010
Publication status	Published - 2 Mar 2023

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Genomics England Research Consortium, Genetti, CA., Pinelli, M., Brunetti-Pierri, N., Garza-Flores, A., Jackson, A., Shahani, D., Saneto, RP., Zampino, G., Leoni, C., Agolini, E., Novelli, A., Haack, BUBTB., Heinritz, W., Matzker, E., Alhaddad, B., Abou Jamra, R., Bartolomaeus, T., AlHamdan, S., ... Chao, HT. (2023). 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, 110(3), 548. https://doi.org/10.1016/j.ajhg.2023.02.010

Genomics England Research Consortium ; Genetti, CA ; Pinelli, M et al. / 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)). In: American Journal of Human Genetics. 2023 ; Vol. 110, No. 3. pp. 548.

@article{5bb96e6dbf494bef9208796742127be1,

title = "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))",

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.",

author = "{Genomics England Research Consortium} and CA Genetti and M Pinelli and N Brunetti-Pierri and A Garza-Flores and Adam Jackson and D Shahani and RP Saneto and G Zampino and C Leoni and E Agolini and A Novelli and BUBTB Haack and W Heinritz and E Matzker and B Alhaddad and {Abou Jamra}, R and T Bartolomaeus and S AlHamdan and R Carapito and B Isidor and S Bahram and A Ritter and K Izumi and B Shakked and O Barel and {Ben Zeev}, B and A Begtrup and DA Carere and SV Mullegama and TB Palculict and DG Calame and K Schwan and ARP Aycinena and R Traberg and S Douzgou and H Pirt and S Banka and HT Chao",

year = "2023",

month = mar,

day = "2",

doi = "10.1016/j.ajhg.2023.02.010",

language = "English",

volume = "110",

pages = "548",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "3",

}

Genomics England Research Consortium, Genetti, CA, Pinelli, M, Brunetti-Pierri, N, Garza-Flores, A, Jackson, A, Shahani, D, Saneto, RP, Zampino, G, Leoni, C, Agolini, E, Novelli, A, Haack, BUBTB, Heinritz, W, Matzker, E, Alhaddad, B, Abou Jamra, R, Bartolomaeus, T, AlHamdan, S, Carapito, R, Isidor, B, Bahram, S, Ritter, A, Izumi, K, Shakked, B, Barel, O, Ben Zeev, B, Begtrup, A, Carere, DA, Mullegama, SV, Palculict, TB, Calame, DG, Schwan, K, Aycinena, ARP, Traberg, R, Douzgou, S, Pirt, H, Banka, S & Chao, HT 2023, '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, vol. 110, no. 3, pp. 548. 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)). / Genomics England Research Consortium; Genetti, CA; Pinelli, M et al.
In: American Journal of Human Genetics, Vol. 110, No. 3, 02.03.2023, p. 548.

Research output: Contribution to journal › Commentary/debate › peer-review

TY - JOUR

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AU - Genetti, CA

AU - Pinelli, M

AU - Brunetti-Pierri, N

AU - Garza-Flores, A

AU - Jackson, Adam

AU - Shahani, D

AU - Saneto, RP

AU - Zampino, G

AU - Leoni, C

AU - Agolini, E

AU - Novelli, A

AU - Haack, BUBTB

AU - Heinritz, W

AU - Matzker, E

AU - Alhaddad, B

AU - Abou Jamra, R

AU - Bartolomaeus, T

AU - AlHamdan, S

AU - Carapito, R

AU - Isidor, B

AU - Bahram, S

AU - Ritter, A

AU - Izumi, K

AU - Shakked, B

AU - Barel, O

AU - Ben Zeev, B

AU - Begtrup, A

AU - Carere, DA

AU - Mullegama, SV

AU - Palculict, TB

AU - Calame, DG

AU - Schwan, K

AU - Aycinena, ARP

AU - Traberg, R

AU - Douzgou, S

AU - Pirt, H

AU - Banka, S

AU - Chao, HT

PY - 2023/3/2

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N2 - (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.

AB - (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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JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

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ER -

Genomics England Research Consortium, Genetti CA, Pinelli M, Brunetti-Pierri N, Garza-Flores A, Jackson A et al. 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. 2023 Mar 2;110(3):548. doi: 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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