Correction: Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

Elke de Boer; Charlotte W Ockeloen; Rosalie A Kampen; Juliet E Hampstead; Alexander J M Dingemans; Dmitrijs Rots; Lukas Lütje; Tazeen Ashraf; Rachel Baker; Mouna Barat-Houari; Brad Angle; Nicolas Chatron; Anne-Sophie Denommé-Pichon; Orrin Devinsky; Christèle Dubourg; Frances Elmslie; Houda Zghal Elloumi; Laurence Faivre; Sarah Fitzgerald-Butt; David Geneviève; Jacqueline A C Goos; Benjamin M Helm; Usha Kini; Amaia Lasa-Aranzasti; Gaetan Lesca; Sally A Lynch; Irene M J Mathijssen; Ruth McGowan; Kristin G Monaghan; Sylvie Odent; Rolph Pfundt; Audrey Putoux; Jeroen van Reeuwijk; Gijs W E Santen; Erina Sasaki; Arthur Sorlin; Peter J van der Spek; Alexander P A Stegmann; Sigrid M A Swagemakers; Irene Valenzuela; Eléonore Viora-Dupont; Antonio Vitobello; Stephanie M Ware; Mathys Wéber; Christian Gilissen; Karen J Low; Simon E Fisher; Lisenka E L M Vissers; Maggie M K Wong; Tjitske Kleefstra

doi:10.1016/j.gim.2023.100962

Correction: Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

Elke de Boer
, Charlotte W Ockeloen^*
, Rosalie A Kampen
, Juliet E Hampstead
, Alexander J M Dingemans
, Dmitrijs Rots
, Lukas Lütje
, Tazeen Ashraf
, Rachel Baker
, Mouna Barat-Houari
, Brad Angle
, Nicolas Chatron
, Anne-Sophie Denommé-Pichon
, Orrin Devinsky
, Christèle Dubourg
, Frances Elmslie
, Houda Zghal Elloumi
, Laurence Faivre
, Sarah Fitzgerald-Butt
, David Geneviève

Jacqueline A C Goos, Benjamin M Helm, Usha Kini, Amaia Lasa-Aranzasti, Gaetan Lesca, Sally A Lynch, Irene M J Mathijssen, Ruth McGowan, Kristin G Monaghan, Sylvie Odent, Rolph Pfundt, Audrey Putoux, Jeroen van Reeuwijk, Gijs W E Santen, Erina Sasaki, Arthur Sorlin, Peter J van der Spek, Alexander P A Stegmann, Sigrid M A Swagemakers, Irene Valenzuela, Eléonore Viora-Dupont, Antonio Vitobello, Stephanie M Ware, Mathys Wéber, Christian Gilissen, Karen J Low, Simon E Fisher, Lisenka E L M Vissers, Maggie M K Wong, Tjitske Kleefstra

^*Corresponding author for this work

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

Abstract

Correction to: Genetics in Medicine 2022; https://doi.org/10.1016/j.gim.2022.06.007, published online 14 July 2022. In the article “Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein” (Genet Med 2022;24:2051–2064), the following update was made. On page 2060, Figure 3 had an error in the artwork (the EGFP and Merged fluorescence imaging of ANKRD11 p.Leu509Pro and p.Arg2512Gln are identical). The revised Figure 3 is shown below. The authors would like to apologize for any inconvenience this may have caused. The article has been corrected online and can be accessed at https://doi.org/10.1016/j.gim.2022.06.007.[Formula

Original language	English
Article number	100962
Number of pages	3
Journal	Genetics in Medicine
Volume	25
Issue number	11
Early online date	1 Sept 2023
DOIs	https://doi.org/10.1016/j.gim.2023.100962
Publication status	Published - Nov 2023

Access to Document

10.1016/j.gim.2023.100962Licence: CC BY

Cite this

de Boer, E., Ockeloen, C. W., Kampen, R. A., Hampstead, J. E., Dingemans, A. J. M., Rots, D., Lütje, L., Ashraf, T., Baker, R., Barat-Houari, M., Angle, B., Chatron, N., Denommé-Pichon, A.-S., Devinsky, O., Dubourg, C., Elmslie, F., Elloumi, H. Z., Faivre, L., Fitzgerald-Butt, S., ... Kleefstra, T. (2023). Correction: Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein. Genetics in Medicine, 25(11), Article 100962. https://doi.org/10.1016/j.gim.2023.100962

@article{a6b6fb353a6245e58dcb13d03a86fcf8,

title = "Correction: Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein",

abstract = "Correction to: Genetics in Medicine 2022; https://doi.org/10.1016/j.gim.2022.06.007, published online 14 July 2022. In the article “Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein” (Genet Med 2022;24:2051–2064), the following update was made. On page 2060, Figure 3 had an error in the artwork (the EGFP and Merged fluorescence imaging of ANKRD11 p.Leu509Pro and p.Arg2512Gln are identical). The revised Figure 3 is shown below. The authors would like to apologize for any inconvenience this may have caused. The article has been corrected online and can be accessed at https://doi.org/10.1016/j.gim.2022.06.007.[Formula",

author = "\{de Boer\}, Elke and Ockeloen, \{Charlotte W\} and Kampen, \{Rosalie A\} and Hampstead, \{Juliet E\} and Dingemans, \{Alexander J M\} and Dmitrijs Rots and Lukas L{\"u}tje and Tazeen Ashraf and Rachel Baker and Mouna Barat-Houari and Brad Angle and Nicolas Chatron and Anne-Sophie Denomm{\'e}-Pichon and Orrin Devinsky and Christ{\`e}le Dubourg and Frances Elmslie and Elloumi, \{Houda Zghal\} and Laurence Faivre and Sarah Fitzgerald-Butt and David Genevi{\`e}ve and Goos, \{Jacqueline A C\} and Helm, \{Benjamin M\} and Usha Kini and Amaia Lasa-Aranzasti and Gaetan Lesca and Lynch, \{Sally A\} and Mathijssen, \{Irene M J\} and Ruth McGowan and Monaghan, \{Kristin G\} and Sylvie Odent and Rolph Pfundt and Audrey Putoux and \{van Reeuwijk\}, Jeroen and Santen, \{Gijs W E\} and Erina Sasaki and Arthur Sorlin and \{van der Spek\}, \{Peter J\} and Stegmann, \{Alexander P A\} and Swagemakers, \{Sigrid M A\} and Irene Valenzuela and El{\'e}onore Viora-Dupont and Antonio Vitobello and Ware, \{Stephanie M\} and Mathys W{\'e}ber and Christian Gilissen and Low, \{Karen J\} and Fisher, \{Simon E\} and Vissers, \{Lisenka E L M\} and Wong, \{Maggie M K\} and Tjitske Kleefstra",

year = "2023",

month = nov,

doi = "10.1016/j.gim.2023.100962",

language = "English",

volume = "25",

journal = "Genetics in Medicine",

issn = "1098-3600",

publisher = "Elsevier B.V.",

number = "11",

}

de Boer, E, Ockeloen, CW, Kampen, RA, Hampstead, JE, Dingemans, AJM, Rots, D, Lütje, L, Ashraf, T, Baker, R, Barat-Houari, M, Angle, B, Chatron, N, Denommé-Pichon, A-S, Devinsky, O, Dubourg, C, Elmslie, F, Elloumi, HZ, Faivre, L, Fitzgerald-Butt, S, Geneviève, D, Goos, JAC, Helm, BM, Kini, U, Lasa-Aranzasti, A, Lesca, G, Lynch, SA, Mathijssen, IMJ, McGowan, R, Monaghan, KG, Odent, S, Pfundt, R, Putoux, A, van Reeuwijk, J, Santen, GWE, Sasaki, E, Sorlin, A, van der Spek, PJ, Stegmann, APA, Swagemakers, SMA, Valenzuela, I, Viora-Dupont, E, Vitobello, A, Ware, SM, Wéber, M, Gilissen, C, Low, KJ, Fisher, SE, Vissers, LELM, Wong, MMK & Kleefstra, T 2023, 'Correction: Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein', Genetics in Medicine, vol. 25, no. 11, 100962. https://doi.org/10.1016/j.gim.2023.100962

TY - JOUR

T1 - Correction: Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

AU - de Boer, Elke

AU - Ockeloen, Charlotte W

AU - Kampen, Rosalie A

AU - Hampstead, Juliet E

AU - Dingemans, Alexander J M

AU - Rots, Dmitrijs

AU - Lütje, Lukas

AU - Ashraf, Tazeen

AU - Baker, Rachel

AU - Barat-Houari, Mouna

AU - Angle, Brad

AU - Chatron, Nicolas

AU - Denommé-Pichon, Anne-Sophie

AU - Devinsky, Orrin

AU - Dubourg, Christèle

AU - Elmslie, Frances

AU - Elloumi, Houda Zghal

AU - Faivre, Laurence

AU - Fitzgerald-Butt, Sarah

AU - Geneviève, David

AU - Goos, Jacqueline A C

AU - Helm, Benjamin M

AU - Kini, Usha

AU - Lasa-Aranzasti, Amaia

AU - Lesca, Gaetan

AU - Lynch, Sally A

AU - Mathijssen, Irene M J

AU - McGowan, Ruth

AU - Monaghan, Kristin G

AU - Odent, Sylvie

AU - Pfundt, Rolph

AU - Putoux, Audrey

AU - van Reeuwijk, Jeroen

AU - Santen, Gijs W E

AU - Sasaki, Erina

AU - Sorlin, Arthur

AU - van der Spek, Peter J

AU - Stegmann, Alexander P A

AU - Swagemakers, Sigrid M A

AU - Valenzuela, Irene

AU - Viora-Dupont, Eléonore

AU - Vitobello, Antonio

AU - Ware, Stephanie M

AU - Wéber, Mathys

AU - Gilissen, Christian

AU - Low, Karen J

AU - Fisher, Simon E

AU - Vissers, Lisenka E L M

AU - Wong, Maggie M K

AU - Kleefstra, Tjitske

PY - 2023/11

Y1 - 2023/11

N2 - Correction to: Genetics in Medicine 2022; https://doi.org/10.1016/j.gim.2022.06.007, published online 14 July 2022. In the article “Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein” (Genet Med 2022;24:2051–2064), the following update was made. On page 2060, Figure 3 had an error in the artwork (the EGFP and Merged fluorescence imaging of ANKRD11 p.Leu509Pro and p.Arg2512Gln are identical). The revised Figure 3 is shown below. The authors would like to apologize for any inconvenience this may have caused. The article has been corrected online and can be accessed at https://doi.org/10.1016/j.gim.2022.06.007.[Formula

AB - Correction to: Genetics in Medicine 2022; https://doi.org/10.1016/j.gim.2022.06.007, published online 14 July 2022. In the article “Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein” (Genet Med 2022;24:2051–2064), the following update was made. On page 2060, Figure 3 had an error in the artwork (the EGFP and Merged fluorescence imaging of ANKRD11 p.Leu509Pro and p.Arg2512Gln are identical). The revised Figure 3 is shown below. The authors would like to apologize for any inconvenience this may have caused. The article has been corrected online and can be accessed at https://doi.org/10.1016/j.gim.2022.06.007.[Formula

U2 - 10.1016/j.gim.2023.100962

DO - 10.1016/j.gim.2023.100962

M3 - Erratum / corrigendum

SN - 1098-3600

VL - 25

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 11

M1 - 100962

ER -

Correction: Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

Abstract

Access to Document

Fingerprint

Cite this