Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Lot Snijders Blok; Justine Rousseau; Joanna Twist; Sophie Ehresmann; Motoki Takaku; Hanka Venselaar; Lance H. Rodan; Catherine B. Nowak; Jessica Douglas; Kathryn J. Swoboda; Marcie A. Steeves; Inderneel Sahai; Connie T. R. M. Stumpel; Alexander P. A. Stegmann; Patricia Wheeler; Marcia Willing; Elise Fiala; Aaina Kochhar; William T. Gibson; Ana S. A. Cohen; Ruky Agbahovbe; A. Micheil Innes; P. Y. Billie Au; Julia Rankin; Ilse J. Anderson; Steven A. Skinner; Raymond J. Louie; Hannah E. Warren; Alexandra Afenjar; Boris Keren; Caroline Nava; Julien Buratti; Arnaud Isapof; Diana Rodriguez; Raymond Lewandowski; Jennifer Propst; Ton van Essen; Murim Choi; Sangmoon Lee; Jong H. Chae; Susan Price; Rhonda E. Schnur; Ganka Douglas; Ingrid M. Wentzensen; Christiane Zweier; André Reis; Martin G. Bialer; Christine Moore; Sandra Jansen; Han G. Brunner; DDD Study; Simon E. Fisher; P.M. Campeau

doi:10.1038/s41467-019-10161-9

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Lot Snijders Blok, Justine Rousseau, Joanna Twist, Sophie Ehresmann, Motoki Takaku, Hanka Venselaar, Lance H. Rodan, Catherine B. Nowak, Jessica Douglas, Kathryn J. Swoboda, Marcie A. Steeves, Inderneel Sahai, Connie T. R. M. Stumpel, Alexander P. A. Stegmann, Patricia Wheeler, Marcia Willing, Elise Fiala, Aaina Kochhar, William T. Gibson, Ana S. A. CohenRuky Agbahovbe, A. Micheil Innes, P. Y. Billie Au, Julia Rankin, Ilse J. Anderson, Steven A. Skinner, Raymond J. Louie, Hannah E. Warren, Alexandra Afenjar, Boris Keren, Caroline Nava, Julien Buratti, Arnaud Isapof, Diana Rodriguez, Raymond Lewandowski, Jennifer Propst, Ton van Essen, Murim Choi, Sangmoon Lee, Jong H. Chae, Susan Price, Rhonda E. Schnur, Ganka Douglas, Ingrid M. Wentzensen, Christiane Zweier, André Reis, Martin G. Bialer, Christine Moore, Sandra Jansen, Han G. Brunner, DDD Study, Simon E. Fisher^*, P.M. Campeau^*

^*Corresponding author for this work

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

Abstract

The HTML and PDF versions of this Article were updated after publication to remove images of one individual from Figure 1.

Original language	English
Article number	2079
Number of pages	4
Journal	Nature Communications
Volume	10
DOIs	https://doi.org/10.1038/s41467-019-10161-9
Publication status	Published - 2 May 2019

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Blok, L. S., Rousseau, J., Twist, J., Ehresmann, S., Takaku, M., Venselaar, H., Rodan, L. H., Nowak, C. B., Douglas, J., Swoboda, K. J., Steeves, M. A., Sahai, I., Stumpel, C. T. R. M., Stegmann, A. P. A., Wheeler, P., Willing, M., Fiala, E., Kochhar, A., Gibson, W. T., Cohen, A. S. A., & 33 othersAgbahovbe, R., Innes, A. M., Au, P. Y. B., Rankin, J., Anderson, I. J., Skinner, S. A., Louie, R. J., Warren, H. E., Afenjar, A., Keren, B., Nava, C., Buratti, J., Isapof, A., Rodriguez, D., Lewandowski, R., Propst, J., van Essen, T., Choi, M., Lee, S., Chae, J. H., Price, S., Schnur, R. E., Douglas, G., Wentzensen, I. M., Zweier, C., Reis, A., Bialer, M. G., Moore, C., Koopmans, M., Brilstra, E. H., DDD Study, Fisher, S. E. & Campeau, P. M., 15 Feb 2019, In: Nature Communications. 10, p. 1-4 4 p., 883.
Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

Open Access
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Blok, L. S., Rousseau, J., Twist, J., Ehresmann, S., Takaku, M., Venselaar, H., Rodan, L. H., Nowak, C. B., Douglas, J., Swoboda, K. J., Steeves, M. A., Sahai, I., Stumpel, C. T. R. M., Stegmann, A. P. A., Wheeler, P., Willing, M., Fiala, E., Kochhar, A., Gibson, W. T., Cohen, A. S. A., & 33 othersAgbahovbe, R., Innes, A. M., Au, P. Y. B., Rankin, J., Anderson, I. J., Skinner, S. A., Louie, R. J., Warren, H. E., Afenjar, A., Keren, B., Nava, C., Buratti, J., Isapof, A., Rodriguez, D., Lewandowski, R., Propst, J., van Essen, T., Choi, M., Lee, S., Chae, J. H., Price, S., Schnur, R. E., Douglas, G., Wentzensen, I. M., Zweier, C., Reis, A., Bialer, M. G., Moore, C., Jansen, S., Brunner, H. G., DDD Study, Campeau, P. M. & Fisher, S. E., 5 Nov 2018, In: Nature Communications. 9, 1, 12 p., 4619.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

Cite this

Snijders Blok, L., Rousseau, J., Twist, J., Ehresmann, S., Takaku, M., Venselaar, H., Rodan, L. H., Nowak, C. B., Douglas, J., Swoboda, K. J., Steeves, M. A., Sahai, I., Stumpel, C. T. R. M., Stegmann, A. P. A., Wheeler, P., Willing, M., Fiala, E., Kochhar, A., Gibson, W. T., ... Campeau, P. M. (2019). Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nature Communications, 10, Article 2079. https://doi.org/10.1038/s41467-019-10161-9

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abstract = "The HTML and PDF versions of this Article were updated after publication to remove images of one individual from Figure 1.",

author = "{Snijders Blok}, Lot and Justine Rousseau and Joanna Twist and Sophie Ehresmann and Motoki Takaku and Hanka Venselaar and Rodan, {Lance H.} and Nowak, {Catherine B.} and Jessica Douglas and Swoboda, {Kathryn J.} and Steeves, {Marcie A.} and Inderneel Sahai and Stumpel, {Connie T. R. M.} and Stegmann, {Alexander P. A.} and Patricia Wheeler and Marcia Willing and Elise Fiala and Aaina Kochhar and Gibson, {William T.} and Cohen, {Ana S. A.} and Ruky Agbahovbe and Innes, {A. Micheil} and Au, {P. Y. Billie} and Julia Rankin and Anderson, {Ilse J.} and Skinner, {Steven A.} and Louie, {Raymond J.} and Warren, {Hannah E.} and Alexandra Afenjar and Boris Keren and Caroline Nava and Julien Buratti and Arnaud Isapof and Diana Rodriguez and Raymond Lewandowski and Jennifer Propst and {van Essen}, Ton and Murim Choi and Sangmoon Lee and Chae, {Jong H.} and Susan Price and Schnur, {Rhonda E.} and Ganka Douglas and Wentzensen, {Ingrid M.} and Christiane Zweier and Andr{\'e} Reis and Bialer, {Martin G.} and Christine Moore and Sandra Jansen and Brunner, {Han G.} and {DDD Study} and Fisher, {Simon E.} and P.M. Campeau",

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Snijders Blok, L, Rousseau, J, Twist, J, Ehresmann, S, Takaku, M, Venselaar, H, Rodan, LH, Nowak, CB, Douglas, J, Swoboda, KJ, Steeves, MA, Sahai, I, Stumpel, CTRM, Stegmann, APA, Wheeler, P, Willing, M, Fiala, E, Kochhar, A, Gibson, WT, Cohen, ASA, Agbahovbe, R, Innes, AM, Au, PYB, Rankin, J, Anderson, IJ, Skinner, SA, Louie, RJ, Warren, HE, Afenjar, A, Keren, B, Nava, C, Buratti, J, Isapof, A, Rodriguez, D, Lewandowski, R, Propst, J, van Essen, T, Choi, M, Lee, S, Chae, JH, Price, S, Schnur, RE, Douglas, G, Wentzensen, IM, Zweier, C, Reis, A, Bialer, MG, Moore, C, Jansen, S, Brunner, HG, DDD Study, Fisher, SE & Campeau, PM 2019, 'Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language', Nature Communications, vol. 10, 2079. https://doi.org/10.1038/s41467-019-10161-9

TY - JOUR

T1 - Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

AU - Snijders Blok, Lot

AU - Rousseau, Justine

AU - Twist, Joanna

AU - Ehresmann, Sophie

AU - Takaku, Motoki

AU - Venselaar, Hanka

AU - Rodan, Lance H.

AU - Nowak, Catherine B.

AU - Douglas, Jessica

AU - Swoboda, Kathryn J.

AU - Steeves, Marcie A.

AU - Sahai, Inderneel

AU - Stumpel, Connie T. R. M.

AU - Stegmann, Alexander P. A.

AU - Wheeler, Patricia

AU - Willing, Marcia

AU - Fiala, Elise

AU - Kochhar, Aaina

AU - Gibson, William T.

AU - Cohen, Ana S. A.

AU - Agbahovbe, Ruky

AU - Innes, A. Micheil

AU - Au, P. Y. Billie

AU - Rankin, Julia

AU - Anderson, Ilse J.

AU - Skinner, Steven A.

AU - Louie, Raymond J.

AU - Warren, Hannah E.

AU - Afenjar, Alexandra

AU - Keren, Boris

AU - Nava, Caroline

AU - Buratti, Julien

AU - Isapof, Arnaud

AU - Rodriguez, Diana

AU - Lewandowski, Raymond

AU - Propst, Jennifer

AU - van Essen, Ton

AU - Choi, Murim

AU - Lee, Sangmoon

AU - Chae, Jong H.

AU - Price, Susan

AU - Schnur, Rhonda E.

AU - Douglas, Ganka

AU - Wentzensen, Ingrid M.

AU - Zweier, Christiane

AU - Reis, André

AU - Bialer, Martin G.

AU - Moore, Christine

AU - Jansen, Sandra

AU - Brunner, Han G.

AU - DDD Study

AU - Fisher, Simon E.

AU - Campeau, P.M.

PY - 2019/5/2

Y1 - 2019/5/2

N2 - The HTML and PDF versions of this Article were updated after publication to remove images of one individual from Figure 1.

AB - The HTML and PDF versions of this Article were updated after publication to remove images of one individual from Figure 1.

U2 - 10.1038/s41467-019-10161-9

DO - 10.1038/s41467-019-10161-9

M3 - Erratum / corrigendum / retractions

SN - 2041-1723

VL - 10

JO - Nature Communications

JF - Nature Communications

M1 - 2079

ER -