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Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant

Publikation: AndetAndet bidragFormidling

Harvard

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

APA

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, jan). Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant. (1 udg.) Genetics in medicine : official journal of the American College of Medical Genetics https://doi.org/10.1038/s41436-020-00969-y

CBE

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. 1 s. 1 udg. https://doi.org/10.1038/s41436-020-00969-y

MLA

Beauregard-Lacroix, Eliane o.a.., Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant, 1 udg., (Genetics in medicine : official journal of the American College of Medical Genetics)., 2021. https://doi.org/10.1038/s41436-020-00969-y

Vancouver

Beauregard-Lacroix E, Pacheco-Cuellar G, Ajeawung NF, Tardif J, Dieterich K, Dabir T o.a. Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant. 2021. 1 s. https://doi.org/10.1038/s41436-020-00969-y

Author

Beauregard-Lacroix, Eliane ; Pacheco-Cuellar, Guillermo ; Ajeawung, Norbert F ; Tardif, Jessica ; Dieterich, Klaus ; Dabir, Tabib ; Vind-Kezunovic, Dina ; White, Susan M ; Zadori, Denes ; Castiglioni, Claudia ; Tranebjærg, Lisbeth ; Tørring, Pernille Mathiesen ; Blair, Ed ; Wisniewska, Marzena ; Camurri, Maria Vittoria ; van Bever, Yolande ; Molidperee, Sirinart ; Taylor, Juliet ; Dionne-Laporte, Alexandre ; Sisodiya, Sanjay M ; Hennekam, Raoul C M ; Campeau, Philippe M. / Correction : DOORS syndrome and a recurrent truncating ATP6V1B2 variant. 2021. 1 s. (Genetics in medicine : official journal of the American College of Medical Genetics).

Bibtex

@misc{0ae1104741754738a60ab09a7ae04234,
title = "Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant",
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}",
year = "2021",
month = jan,
doi = "10.1038/s41436-020-00969-y",
language = "English",
volume = "23",
series = "Genetics in medicine : official journal of the American College of Medical Genetics",
publisher = "Lippincott Williams & Wilkins",
edition = "1",
type = "Other",

}

RIS

TY - GEN

T1 - Correction

T2 - DOORS syndrome and a recurrent truncating ATP6V1B2 variant

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.

UR - http://www.scopus.com/inward/record.url?scp=85090978565&partnerID=8YFLogxK

U2 - 10.1038/s41436-020-00969-y

DO - 10.1038/s41436-020-00969-y

M3 - Other contribution

C2 - 32934366

VL - 23

T3 - Genetics in medicine : official journal of the American College of Medical Genetics

ER -

ID: 61245580