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

L.S. Blok, J. Rousseau, J. Twist, S. Ehresmann, M. Takaku, H. Venselaar, L.H. Rodan, C.B. Nowak, J. Douglas, K.J. Swoboda, M.A. Steeves, I. Sahai, C.T.R.M. Stumpel, A.P.A. Stegmann, P. Wheeler, M. Willing, E. Fiala, A. Kochhar, W.T. Gibson, A.S.A. CohenR. Agbahovbe, A.M. Innes, P.Y.B. Au, J. Rankin, I.J. Anderson, S.A. Skinner, R.J. Louie, H.E. Warren, A. Afenjar, B. Keren, C. Nava, J. Buratti, A. Isapof, D. Rodriguez, R. Lewandowski, J. Propst, T. van Essen, M. Choi, S. Lee, J.H. Chae, S. Price, R.E. Schnur, G. Douglas, I.M. Wentzensen, C. Zweier, A. Reis, M.G. Bialer, C. Moore, M. Koopmans, E.H. Brilstra, DDD Study, Simon E. Fisher*, Philippe M. Campeau*

*Corresponding author for this work

Research output: Contribution to journalErratum / corrigendum / retractionsAcademic

Abstract

The original version of this Article contained an error in the spelling of the author Laurence Faivre, which was incorrectly given as Laurence Faive. This has now been corrected in both the PDF and HTML versions of the Article.
Original languageEnglish
Article number883
Pages (from-to)1-4
Number of pages4
JournalNature Communications
Volume10
DOIs
Publication statusPublished - 15 Feb 2019
  • Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

    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., 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, Fisher, S. E. & Campeau, P. M., 2 May 2019, In: Nature Communications. 10, 4 p., 2079.

    Research output: Contribution to journalErratum / corrigendum / retractionsAcademic

    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 journalArticleAcademicpeer-review

    Open Access

Cite this