Erratum: Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy (The American Journal of Human Genetics (2021) 108(4) (739–748), (S0002929721000574), (10.1016/j.ajhg.2021.02.015))

Ambrin Fatima; Jan Hoeber; Jens Schuster; Eriko Koshimizu; Carolina Maya-Gonzalez; Boris Keren; Cyril Mignot; Talia Akram; Zafar Ali; Satoko Miyatake; Junpei Tanigawa; Takayoshi Koike; Mitsuhiro Kato; Yoshiko Murakami; Uzma Abdullah; Muhammad Akhtar Ali; Rein Fadoul; Loora Laan; Casimiro Castillejo-López; Maarika Liik; Zhe Jin; Bryndis Birnir; Naomichi Matsumoto; Shahid M. Baig; Joakim Klar; Niklas Dahl

doi:10.1016/j.ajhg.2022.02.007

Erratum: Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy (The American Journal of Human Genetics (2021) 108(4) (739–748), (S0002929721000574), (10.1016/j.ajhg.2021.02.015))

Ambrin Fatima
, Jan Hoeber
, Jens Schuster
, Eriko Koshimizu
, Carolina Maya-Gonzalez
, Boris Keren
, Cyril Mignot
, Talia Akram
, Zafar Ali
, Satoko Miyatake
, Junpei Tanigawa
, Takayoshi Koike
, Mitsuhiro Kato
, Yoshiko Murakami
, Uzma Abdullah
, Muhammad Akhtar Ali
, Rein Fadoul
, Loora Laan
, Casimiro Castillejo-López
, Maarika Liik

Zhe Jin, Bryndis Birnir, Naomichi Matsumoto, Shahid M. Baig, Joakim Klar, Niklas Dahl

Department of Biological & Biomedical Sciences, Medical College, Pakistan

Research output: Contribution to journal › Comment/debate

Abstract

(The American Journal of Human Genetics 108, 739–748; April 1, 2021) In the originally published version of this article, family 2 was assigned an incorrect aa substitution as a result of the G>A transition in codon 478 of the NCDN gene. The aa substitution in individual F2: II.1 should read p.Arg478Gln, not p.Arg478Glu. The error appeared consistently throughout the text, in Table 1, and in Figures 1, 2, and 3; the error has been corrected online and Figures 1, 2, and 3 appear correctly here as well. The authors regret this error.

Original language	English (US)
Pages (from-to)	542-546
Number of pages	5
Journal	American Journal of Human Genetics
Volume	109
Issue number	3
DOIs	https://doi.org/10.1016/j.ajhg.2022.02.007
Publication status	Published - 3 Mar 2022

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Fatima, A., Hoeber, J., Schuster, J., Koshimizu, E., Maya-Gonzalez, C., Keren, B., Mignot, C., Akram, T., Ali, Z., Miyatake, S., Tanigawa, J., Koike, T., Kato, M., Murakami, Y., Abdullah, U., Ali, M. A., Fadoul, R., Laan, L., Castillejo-López, C., ... Dahl, N. (2022). Erratum: Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy (The American Journal of Human Genetics (2021) 108(4) (739–748), (S0002929721000574), (10.1016/j.ajhg.2021.02.015)). American Journal of Human Genetics, 109(3), 542-546. https://doi.org/10.1016/j.ajhg.2022.02.007

Fatima, Ambrin ; Hoeber, Jan ; Schuster, Jens et al. / Erratum : Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy (The American Journal of Human Genetics (2021) 108(4) (739–748), (S0002929721000574), (10.1016/j.ajhg.2021.02.015)). In: American Journal of Human Genetics. 2022 ; Vol. 109, No. 3. pp. 542-546.

@article{7a07abd279d14fb581be147f430ae19e,

title = "Erratum: Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy (The American Journal of Human Genetics (2021) 108(4) (739–748), (S0002929721000574), (10.1016/j.ajhg.2021.02.015))",

abstract = "(The American Journal of Human Genetics 108, 739–748; April 1, 2021) In the originally published version of this article, family 2 was assigned an incorrect aa substitution as a result of the G>A transition in codon 478 of the NCDN gene. The aa substitution in individual F2: II.1 should read p.Arg478Gln, not p.Arg478Glu. The error appeared consistently throughout the text, in Table 1, and in Figures 1, 2, and 3; the error has been corrected online and Figures 1, 2, and 3 appear correctly here as well. The authors regret this error.",

author = "Ambrin Fatima and Jan Hoeber and Jens Schuster and Eriko Koshimizu and Carolina Maya-Gonzalez and Boris Keren and Cyril Mignot and Talia Akram and Zafar Ali and Satoko Miyatake and Junpei Tanigawa and Takayoshi Koike and Mitsuhiro Kato and Yoshiko Murakami and Uzma Abdullah and Ali, \{Muhammad Akhtar\} and Rein Fadoul and Loora Laan and Casimiro Castillejo-L{\'o}pez and Maarika Liik and Zhe Jin and Bryndis Birnir and Naomichi Matsumoto and Baig, \{Shahid M.\} and Joakim Klar and Niklas Dahl",

note = "Publisher Copyright: {\textcopyright} 2022 The Author(s)",

year = "2022",

month = mar,

day = "3",

doi = "10.1016/j.ajhg.2022.02.007",

language = "English (US)",

volume = "109",

pages = "542--546",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "3",

}

Fatima, A, Hoeber, J, Schuster, J, Koshimizu, E, Maya-Gonzalez, C, Keren, B, Mignot, C, Akram, T, Ali, Z, Miyatake, S, Tanigawa, J, Koike, T, Kato, M, Murakami, Y, Abdullah, U, Ali, MA, Fadoul, R, Laan, L, Castillejo-López, C, Liik, M, Jin, Z, Birnir, B, Matsumoto, N, Baig, SM, Klar, J & Dahl, N 2022, 'Erratum: Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy (The American Journal of Human Genetics (2021) 108(4) (739–748), (S0002929721000574), (10.1016/j.ajhg.2021.02.015))', American Journal of Human Genetics, vol. 109, no. 3, pp. 542-546. https://doi.org/10.1016/j.ajhg.2022.02.007

Erratum: Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy (The American Journal of Human Genetics (2021) 108(4) (739–748), (S0002929721000574), (10.1016/j.ajhg.2021.02.015)). / Fatima, Ambrin; Hoeber, Jan; Schuster, Jens et al.
In: American Journal of Human Genetics, Vol. 109, No. 3, 03.03.2022, p. 542-546.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Erratum

T2 - Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy (The American Journal of Human Genetics (2021) 108(4) (739–748), (S0002929721000574), (10.1016/j.ajhg.2021.02.015))

AU - Fatima, Ambrin

AU - Hoeber, Jan

AU - Schuster, Jens

AU - Koshimizu, Eriko

AU - Maya-Gonzalez, Carolina

AU - Keren, Boris

AU - Mignot, Cyril

AU - Akram, Talia

AU - Ali, Zafar

AU - Miyatake, Satoko

AU - Tanigawa, Junpei

AU - Koike, Takayoshi

AU - Kato, Mitsuhiro

AU - Murakami, Yoshiko

AU - Abdullah, Uzma

AU - Ali, Muhammad Akhtar

AU - Fadoul, Rein

AU - Laan, Loora

AU - Castillejo-López, Casimiro

AU - Liik, Maarika

AU - Jin, Zhe

AU - Birnir, Bryndis

AU - Matsumoto, Naomichi

AU - Baig, Shahid M.

AU - Klar, Joakim

AU - Dahl, Niklas

PY - 2022/3/3

Y1 - 2022/3/3

N2 - (The American Journal of Human Genetics 108, 739–748; April 1, 2021) In the originally published version of this article, family 2 was assigned an incorrect aa substitution as a result of the G>A transition in codon 478 of the NCDN gene. The aa substitution in individual F2: II.1 should read p.Arg478Gln, not p.Arg478Glu. The error appeared consistently throughout the text, in Table 1, and in Figures 1, 2, and 3; the error has been corrected online and Figures 1, 2, and 3 appear correctly here as well. The authors regret this error.

AB - (The American Journal of Human Genetics 108, 739–748; April 1, 2021) In the originally published version of this article, family 2 was assigned an incorrect aa substitution as a result of the G>A transition in codon 478 of the NCDN gene. The aa substitution in individual F2: II.1 should read p.Arg478Gln, not p.Arg478Glu. The error appeared consistently throughout the text, in Table 1, and in Figures 1, 2, and 3; the error has been corrected online and Figures 1, 2, and 3 appear correctly here as well. The authors regret this error.

UR - https://www.scopus.com/pages/publications/85125238528

U2 - 10.1016/j.ajhg.2022.02.007

DO - 10.1016/j.ajhg.2022.02.007

M3 - Comment/debate

C2 - 35245475

AN - SCOPUS:85125238528

SN - 0002-9297

VL - 109

SP - 542

EP - 546

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 3

ER -

Fatima A, Hoeber J, Schuster J, Koshimizu E, Maya-Gonzalez C, Keren B et al. Erratum: Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy (The American Journal of Human Genetics (2021) 108(4) (739–748), (S0002929721000574), (10.1016/j.ajhg.2021.02.015)). American Journal of Human Genetics. 2022 Mar 3;109(3):542-546. doi: 10.1016/j.ajhg.2022.02.007

Erratum: Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy (The American Journal of Human Genetics (2021) 108(4) (739–748), (S0002929721000574), (10.1016/j.ajhg.2021.02.015))

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