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

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. / Snijders Blok, Lot; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H; Nowak, Catherine B; Douglas, Jessica; Swoboda, Kathryn J; Steeves, Marcie A; Sahai, Inderneel; Stumpel, Connie T R M; Stegmann, Alexander P A; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T; Cohen, Ana S A; Agbahovbe, Ruky; Innes, A Micheil; Au, P Y Billie; Rankin, Julia; Anderson, Ilse J; Skinner, Steven A; Louie, Raymond J; Warren, Hannah E; Afenjar, Alexandra; Keren, Boris; Nava, Caroline; Buratti, Julien; Isapof, Arnaud; Rodriguez, Diana; Lewandowski, Raymond; Propst, Jennifer; van Essen, Ton; Choi, Murim; Lee, Sangmoon; Chae, Jong H; Price, Susan; Schnur, Rhonda E; Douglas, Ganka; Wentzensen, Ingrid M; Zweier, Christiane; Reis, André; Bialer, Martin G; Moore, Christine; Koopmans, Marije; Brilstra, Eva H; Monroe, Glen R; van Gassen, Koen L I; van Binsbergen, Ellen; Newbury-Ecob, Ruth; Bownass, Lucy; Bader, Ingrid; Mayr, Johannes A; Wortmann, Saskia B; Jakielski, Kathy J; Strand, Edythe A; Kloth, Katja; Bierhals, Tatjana; DDD Study; Roberts, John D; Petrovich, Robert M; Machida, Shinichi; Kurumizaka, Hitoshi; Lelieveld, Stefan; Pfundt, Rolph; Jansen, Sandra; Deriziotis, Pelagia; Faivre, Laurence; Thevenon, Julien; Assoum, Mirna; Shriberg, Lawrence; Kleefstra, Tjitske; Brunner, Han G; Wade, Paul A; Fisher, Simon E; Campeau, Philippe M.

In: NAT COMMUN, Vol. 10, No. 1, 02.05.2019, p. 2079.

Research output: SCORING: Contribution to journalOther (editorial matter etc.)Research

Harvard

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, Koopmans, M, Brilstra, EH, Monroe, GR, van Gassen, KLI, van Binsbergen, E, Newbury-Ecob, R, Bownass, L, Bader, I, Mayr, JA, Wortmann, SB, Jakielski, KJ, Strand, EA, Kloth, K, Bierhals, T, DDD Study, Roberts, JD, Petrovich, RM, Machida, S, Kurumizaka, H, Lelieveld, S, Pfundt, R, Jansen, S, Deriziotis, P, Faivre, L, Thevenon, J, Assoum, M, Shriberg, L, Kleefstra, T, Brunner, HG, Wade, PA, Fisher, SE & Campeau, PM 2019, 'Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language', NAT COMMUN, vol. 10, no. 1, pp. 2079. https://doi.org/10.1038/s41467-019-10161-9

APA

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. NAT COMMUN, 10(1), 2079. https://doi.org/10.1038/s41467-019-10161-9

Vancouver

Bibtex

@article{b1d86ea6d4424c4f8348a2292e3e3538,
title = "Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language",
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 Marije Koopmans and Brilstra, {Eva H} and Monroe, {Glen R} and {van Gassen}, {Koen L I} and {van Binsbergen}, Ellen and Ruth Newbury-Ecob and Lucy Bownass and Ingrid Bader and Mayr, {Johannes A} and Wortmann, {Saskia B} and Jakielski, {Kathy J} and Strand, {Edythe A} and Katja Kloth and Tatjana Bierhals and {DDD Study} and Roberts, {John D} and Petrovich, {Robert M} and Shinichi Machida and Hitoshi Kurumizaka and Stefan Lelieveld and Rolph Pfundt and Sandra Jansen and Pelagia Deriziotis and Laurence Faivre and Julien Thevenon and Mirna Assoum and Lawrence Shriberg and Tjitske Kleefstra and Brunner, {Han G} and Wade, {Paul A} and Fisher, {Simon E} and Campeau, {Philippe M}",
year = "2019",
month = may,
day = "2",
doi = "10.1038/s41467-019-10161-9",
language = "English",
volume = "10",
pages = "2079",
journal = "NAT COMMUN",
issn = "2041-1723",
publisher = "NATURE PUBLISHING GROUP",
number = "1",

}

RIS

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 - Koopmans, Marije

AU - Brilstra, Eva H

AU - Monroe, Glen R

AU - van Gassen, Koen L I

AU - van Binsbergen, Ellen

AU - Newbury-Ecob, Ruth

AU - Bownass, Lucy

AU - Bader, Ingrid

AU - Mayr, Johannes A

AU - Wortmann, Saskia B

AU - Jakielski, Kathy J

AU - Strand, Edythe A

AU - Kloth, Katja

AU - Bierhals, Tatjana

AU - DDD Study

AU - Roberts, John D

AU - Petrovich, Robert M

AU - Machida, Shinichi

AU - Kurumizaka, Hitoshi

AU - Lelieveld, Stefan

AU - Pfundt, Rolph

AU - Jansen, Sandra

AU - Deriziotis, Pelagia

AU - Faivre, Laurence

AU - Thevenon, Julien

AU - Assoum, Mirna

AU - Shriberg, Lawrence

AU - Kleefstra, Tjitske

AU - Brunner, Han G

AU - Wade, Paul A

AU - Fisher, Simon E

AU - Campeau, Philippe 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 - Other (editorial matter etc.)

C2 - 31048695

VL - 10

SP - 2079

JO - NAT COMMUN

JF - NAT COMMUN

SN - 2041-1723

IS - 1

ER -