Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency (Genetics in Medicine, (2021), 23, 9, (1705-1714), 10.1038/s41436-021-01194-x)

Saskia B. Wortmann; Szymon Ziętkiewicz; Sergio Guerrero-Castillo; René G. Feichtinger; Matias Wagner; Jacqui Russell; Carolyn Ellaway; Dagmara Mróz; Hubert Wyszkowski; Denisa Weis; Iris Hannibal; Celina von Stülpnagel; Alfredo Cabrera-Orefice; Uta Lichter-Konecki; Jenna Gaesser; Randy Windreich; Kasiani C. Myers; Robert Lorsbach; Russell C. Dale; Søren Gersting; Carlos E. Prada; John Christodoulou; Nicole I. Wolf; Hanka Venselaar; Johannes A. Mayr; Ron A. Wevers

doi:https://doi.org/10.1038/s41436-021-01280-0

Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency (Genetics in Medicine, (2021), 23, 9, (1705-1714), 10.1038/s41436-021-01194-x)

Saskia B. Wortmann, Szymon Ziętkiewicz, Sergio Guerrero-Castillo, René G. Feichtinger, Matias Wagner, Jacqui Russell, Carolyn Ellaway, Dagmara Mróz, Hubert Wyszkowski, Denisa Weis, Iris Hannibal, Celina von Stülpnagel, Alfredo Cabrera-Orefice, Uta Lichter-Konecki, Jenna Gaesser, Randy Windreich, Kasiani C. Myers, Robert Lorsbach, Russell C. Dale, Søren GerstingCarlos E. Prada, John Christodoulou, Nicole I. Wolf, Hanka Venselaar, Johannes A. Mayr, Ron A. Wevers

Research output: Contribution to journal › Comment/Letter to the editor › Academic

Abstract

Unfortunately the funding information was not given. Funding is as follows: This work was funded by the ERA PerMed project PerMiM (Austrian Science Fund FWF, I4704-B) to S.B.W. This study was supported by a “Sonata Bis 5” grant of the National Science Center Poland (2015/18/E/NZ1/00673) to S.Z. and D.M.

Original language	English
Pages (from-to)	1789
Number of pages	1
Journal	Genetics in medicine
Volume	23
Issue number	9
Early online date	2021
DOIs	https://doi.org/10.1038/s41436-021-01280-0
Publication status	Published - Sept 2021

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https://doi.org/10.1038/s41436-021-01280-0

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Wortmann, S. B., Ziętkiewicz, S., Guerrero-Castillo, S., Feichtinger, R. G., Wagner, M., Russell, J., Ellaway, C., Mróz, D., Wyszkowski, H., Weis, D., Hannibal, I., von Stülpnagel, C., Cabrera-Orefice, A., Lichter-Konecki, U., Gaesser, J., Windreich, R., Myers, K. C., Lorsbach, R., Dale, R. C., ... Wevers, R. A. (2021). Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency (Genetics in Medicine, (2021), 23, 9, (1705-1714), 10.1038/s41436-021-01194-x). Genetics in medicine, 23(9), 1789. https://doi.org/10.1038/s41436-021-01280-0

@article{10d3e88ed6a84cf3bc01ab81aa0aff99,

title = "Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency (Genetics in Medicine, (2021), 23, 9, (1705-1714), 10.1038/s41436-021-01194-x)",

abstract = "Unfortunately the funding information was not given. Funding is as follows: This work was funded by the ERA PerMed project PerMiM (Austrian Science Fund FWF, I4704-B) to S.B.W. This study was supported by a “Sonata Bis 5” grant of the National Science Center Poland (2015/18/E/NZ1/00673) to S.Z. and D.M.",

author = "Wortmann, {Saskia B.} and Szymon Zi{\c e}tkiewicz and Sergio Guerrero-Castillo and Feichtinger, {Ren{\'e} G.} and Matias Wagner and Jacqui Russell and Carolyn Ellaway and Dagmara Mr{\'o}z and Hubert Wyszkowski and Denisa Weis and Iris Hannibal and {von St{\"u}lpnagel}, Celina and Alfredo Cabrera-Orefice and Uta Lichter-Konecki and Jenna Gaesser and Randy Windreich and Myers, {Kasiani C.} and Robert Lorsbach and Dale, {Russell C.} and S{\o}ren Gersting and Prada, {Carlos E.} and John Christodoulou and Wolf, {Nicole I.} and Hanka Venselaar and Mayr, {Johannes A.} and Wevers, {Ron A.}",

note = "Funding Information: This study was supported by a “Sonata Bis 5” grant of the National Science Center Poland (2015/18/E/NZ1/00673) to S.Z. and D.M. Funding Information: Correction to: Genetics in Medicine 2021; https://doi.org/10.1038/ s41436-021-01194-x; published online 17 June 2021 Unfortunately the funding information was not given. Funding is as follows: This work was funded by the ERA PerMed project PerMiM (Austrian Science Fund FWF, I4704-B) to S.B.W. Publisher Copyright: {\textcopyright} 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics.",

year = "2021",

month = sep,

doi = "https://doi.org/10.1038/s41436-021-01280-0",

language = "English",

volume = "23",

pages = "1789",

journal = "Genetics in medicine",

issn = "1098-3600",

publisher = "Lippincott Williams and Wilkins",

number = "9",

}

Wortmann, SB, Ziętkiewicz, S, Guerrero-Castillo, S, Feichtinger, RG, Wagner, M, Russell, J, Ellaway, C, Mróz, D, Wyszkowski, H, Weis, D, Hannibal, I, von Stülpnagel, C, Cabrera-Orefice, A, Lichter-Konecki, U, Gaesser, J, Windreich, R, Myers, KC, Lorsbach, R, Dale, RC, Gersting, S, Prada, CE, Christodoulou, J, Wolf, NI, Venselaar, H, Mayr, JA & Wevers, RA 2021, 'Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency (Genetics in Medicine, (2021), 23, 9, (1705-1714), 10.1038/s41436-021-01194-x)', Genetics in medicine, vol. 23, no. 9, pp. 1789. https://doi.org/10.1038/s41436-021-01280-0

Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency (Genetics in Medicine, (2021), 23, 9, (1705-1714), 10.1038/s41436-021-01194-x). / Wortmann, Saskia B.; Ziętkiewicz, Szymon; Guerrero-Castillo, Sergio et al.
In: Genetics in medicine, Vol. 23, No. 9, 09.2021, p. 1789.

Research output: Contribution to journal › Comment/Letter to the editor › Academic

TY - JOUR

T1 - Correction to

T2 - Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency (Genetics in Medicine, (2021), 23, 9, (1705-1714), 10.1038/s41436-021-01194-x)

AU - Wortmann, Saskia B.

AU - Ziętkiewicz, Szymon

AU - Guerrero-Castillo, Sergio

AU - Feichtinger, René G.

AU - Wagner, Matias

AU - Russell, Jacqui

AU - Ellaway, Carolyn

AU - Mróz, Dagmara

AU - Wyszkowski, Hubert

AU - Weis, Denisa

AU - Hannibal, Iris

AU - von Stülpnagel, Celina

AU - Cabrera-Orefice, Alfredo

AU - Lichter-Konecki, Uta

AU - Gaesser, Jenna

AU - Windreich, Randy

AU - Myers, Kasiani C.

AU - Lorsbach, Robert

AU - Dale, Russell C.

AU - Gersting, Søren

AU - Prada, Carlos E.

AU - Christodoulou, John

AU - Wolf, Nicole I.

AU - Venselaar, Hanka

AU - Mayr, Johannes A.

AU - Wevers, Ron A.

N1 - Funding Information: This study was supported by a “Sonata Bis 5” grant of the National Science Center Poland (2015/18/E/NZ1/00673) to S.Z. and D.M. Funding Information: Correction to: Genetics in Medicine 2021; https://doi.org/10.1038/ s41436-021-01194-x; published online 17 June 2021 Unfortunately the funding information was not given. Funding is as follows: This work was funded by the ERA PerMed project PerMiM (Austrian Science Fund FWF, I4704-B) to S.B.W. Publisher Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics.

PY - 2021/9

Y1 - 2021/9

N2 - Unfortunately the funding information was not given. Funding is as follows: This work was funded by the ERA PerMed project PerMiM (Austrian Science Fund FWF, I4704-B) to S.B.W. This study was supported by a “Sonata Bis 5” grant of the National Science Center Poland (2015/18/E/NZ1/00673) to S.Z. and D.M.

AB - Unfortunately the funding information was not given. Funding is as follows: This work was funded by the ERA PerMed project PerMiM (Austrian Science Fund FWF, I4704-B) to S.B.W. This study was supported by a “Sonata Bis 5” grant of the National Science Center Poland (2015/18/E/NZ1/00673) to S.Z. and D.M.

UR - http://www.scopus.com/inward/record.url?scp=85111657647&partnerID=8YFLogxK

U2 - https://doi.org/10.1038/s41436-021-01280-0

DO - https://doi.org/10.1038/s41436-021-01280-0

M3 - Comment/Letter to the editor

C2 - 34302123

SN - 1098-3600

VL - 23

SP - 1789

JO - Genetics in medicine

JF - Genetics in medicine

IS - 9

ER -

Wortmann SB, Ziętkiewicz S, Guerrero-Castillo S, Feichtinger RG, Wagner M, Russell J et al. Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency (Genetics in Medicine, (2021), 23, 9, (1705-1714), 10.1038/s41436-021-01194-x). Genetics in medicine. 2021 Sept;23(9):1789. Epub 2021. doi: https://doi.org/10.1038/s41436-021-01280-0

Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency (Genetics in Medicine, (2021), 23, 9, (1705-1714), 10.1038/s41436-021-01194-x)

Abstract

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