Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2020), 10.1038/s41436-020-00950-9): DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2021), 23, 1, (149-154), 10.1038/s41436-020-00950-9)

Eliane Beauregard-Lacroix; Guillermo Pacheco-Cuellar; Norbert F. Ajeawung; Jessica Tardif; Klaus Dieterich; Tabib Dabir; Dina Vind-Kezunovic; Susan M. White; Denes Zadori; Claudia Castiglioni; Lisbeth Tranebjærg; Pernille Mathiesen Tørring; Ed Blair; Marzena Wisniewska; Maria Vittoria Camurri; Yolande van Bever; Sirinart Molidperee; Juliet Taylor; Alexandre Dionne-Laporte; Sanjay M. Sisodiya; Raoul C. M. Hennekam; Philippe M. Campeau

doi:https://doi.org/10.1038/s41436-020-00969-y

Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2020), 10.1038/s41436-020-00950-9): DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2021), 23, 1, (149-154), 10.1038/s41436-020-00950-9)

Eliane Beauregard-Lacroix, Guillermo Pacheco-Cuellar, Norbert F. Ajeawung, Jessica Tardif, Klaus Dieterich, Tabib Dabir, Dina Vind-Kezunovic, Susan M. White, Denes Zadori, Claudia Castiglioni, Lisbeth Tranebjærg, Pernille Mathiesen Tørring, Ed Blair, Marzena Wisniewska, Maria Vittoria Camurri, Yolande van Bever, Sirinart Molidperee, Juliet Taylor, Alexandre Dionne-Laporte, Sanjay M. SisodiyaRaoul C. M. Hennekam, Philippe M. Campeau

Research output: Contribution to journal › Erratum/Corrigendum › Academic

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Original language	English
Pages (from-to)	237
Number of pages	1
Journal	Genetics in medicine
Volume	23
Issue number	1
Early online date	2020
DOIs	https://doi.org/10.1038/s41436-020-00969-y
Publication status	Published - Jan 2021

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https://doi.org/10.1038/s41436-020-00969-y

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Beauregard-Lacroix, E., Pacheco-Cuellar, G., Ajeawung, N. F., Tardif, J., Dieterich, K., Dabir, T., Vind-Kezunovic, D., White, S. M., Zadori, D., Castiglioni, C., Tranebjærg, L., Tørring, P. M., Blair, E., Wisniewska, M., Camurri, M. V., van Bever, Y., Molidperee, S., Taylor, J., Dionne-Laporte, A., ... Campeau, P. M. (2021). Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2020), 10.1038/s41436-020-00950-9): DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2021), 23, 1, (149-154), 10.1038/s41436-020-00950-9). Genetics in medicine, 23(1), 237. https://doi.org/10.1038/s41436-020-00969-y

Beauregard-Lacroix, Eliane ; Pacheco-Cuellar, Guillermo ; Ajeawung, Norbert F. et al. / Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2020), 10.1038/s41436-020-00950-9) : DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2021), 23, 1, (149-154), 10.1038/s41436-020-00950-9). In: Genetics in medicine. 2021 ; Vol. 23, No. 1. pp. 237.

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title = "Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2020), 10.1038/s41436-020-00950-9): DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2021), 23, 1, (149-154), 10.1038/s41436-020-00950-9)",

abstract = "An amendment to this paper has been published and can be accessed via a link at the top of the paper.",

author = "Eliane Beauregard-Lacroix and Guillermo Pacheco-Cuellar and Ajeawung, {Norbert F.} and Jessica Tardif and Klaus Dieterich and Tabib Dabir and Dina Vind-Kezunovic and White, {Susan M.} and Denes Zadori and Claudia Castiglioni and Lisbeth Tranebj{\ae}rg and T{\o}rring, {Pernille Mathiesen} and Ed Blair and Marzena Wisniewska and Camurri, {Maria Vittoria} and {van Bever}, Yolande and Sirinart Molidperee and Juliet Taylor and Alexandre Dionne-Laporte and Sisodiya, {Sanjay M.} and Hennekam, {Raoul C. M.} and Campeau, {Philippe M.}",

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Beauregard-Lacroix, E, Pacheco-Cuellar, G, Ajeawung, NF, Tardif, J, Dieterich, K, Dabir, T, Vind-Kezunovic, D, White, SM, Zadori, D, Castiglioni, C, Tranebjærg, L, Tørring, PM, Blair, E, Wisniewska, M, Camurri, MV, van Bever, Y, Molidperee, S, Taylor, J, Dionne-Laporte, A, Sisodiya, SM, Hennekam, RCM & Campeau, PM 2021, 'Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2020), 10.1038/s41436-020-00950-9): DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2021), 23, 1, (149-154), 10.1038/s41436-020-00950-9)', Genetics in medicine, vol. 23, no. 1, pp. 237. https://doi.org/10.1038/s41436-020-00969-y

Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2020), 10.1038/s41436-020-00950-9): DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2021), 23, 1, (149-154), 10.1038/s41436-020-00950-9). / Beauregard-Lacroix, Eliane; Pacheco-Cuellar, Guillermo; Ajeawung, Norbert F. et al.
In: Genetics in medicine, Vol. 23, No. 1, 01.2021, p. 237.

Research output: Contribution to journal › Erratum/Corrigendum › Academic

TY - JOUR

T1 - Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2020), 10.1038/s41436-020-00950-9)

T2 - DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2021), 23, 1, (149-154), 10.1038/s41436-020-00950-9)

AU - Beauregard-Lacroix, Eliane

AU - Pacheco-Cuellar, Guillermo

AU - Ajeawung, Norbert F.

AU - Tardif, Jessica

AU - Dieterich, Klaus

AU - Dabir, Tabib

AU - Vind-Kezunovic, Dina

AU - White, Susan M.

AU - Zadori, Denes

AU - Castiglioni, Claudia

AU - Tranebjærg, Lisbeth

AU - Tørring, Pernille Mathiesen

AU - Blair, Ed

AU - Wisniewska, Marzena

AU - Camurri, Maria Vittoria

AU - van Bever, Yolande

AU - Molidperee, Sirinart

AU - Taylor, Juliet

AU - Dionne-Laporte, Alexandre

AU - Sisodiya, Sanjay M.

AU - Hennekam, Raoul C. M.

AU - Campeau, Philippe M.

PY - 2021/1

Y1 - 2021/1

N2 - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

AB - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

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DO - https://doi.org/10.1038/s41436-020-00969-y

M3 - Erratum/Corrigendum

C2 - 32934366

SN - 1098-3600

VL - 23

SP - 237

JO - Genetics in medicine

JF - Genetics in medicine

IS - 1

ER -

Beauregard-Lacroix E, Pacheco-Cuellar G, Ajeawung NF, Tardif J, Dieterich K, Dabir T et al. Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2020), 10.1038/s41436-020-00950-9): DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2021), 23, 1, (149-154), 10.1038/s41436-020-00950-9). Genetics in medicine. 2021 Jan;23(1):237. Epub 2020. doi: https://doi.org/10.1038/s41436-020-00969-y

Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2020), 10.1038/s41436-020-00950-9): DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2021), 23, 1, (149-154), 10.1038/s41436-020-00950-9)

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