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 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

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DOI: 10.1038/s41467-019-10161-9
Published: 2019 May 2
Container: Nature communications
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1038/s41467-019-10161-9,
  title = {Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.},
  author = {Snijders Blok L and Rousseau J and Twist J and Ehresmann S and Takaku M and Venselaar H and Rodan LH and Nowak CB and Douglas J and Swoboda KJ and Steeves MA and Sahai I and Stumpel CTRM and Stegmann APA and Wheeler P and Willing M and Fiala E and Kochhar A and Gibson WT and Cohen ASA and Agbahovbe R and Innes AM and Au PYB and Rankin J and Anderson IJ and Skinner SA and Louie RJ and Warren HE and Afenjar A and Keren B and Nava C and Buratti J and Isapof A and Rodriguez D and Lewandowski R and Propst J and van Essen T and Choi M and Lee S and Chae JH and Price S and Schnur RE and Douglas G and Wentzensen IM and Zweier C and Reis A and Bialer MG and Moore C and Koopmans M and Brilstra EH and Monroe GR and van Gassen KLI and van Binsbergen E and Newbury-Ecob R and Bownass L and Bader I and Mayr JA and Wortmann SB and Jakielski KJ and Strand EA and Kloth K and Bierhals T and DDD study and Roberts JD and Petrovich RM and Machida S and Kurumizaka H and Lelieveld S and Pfundt R and Jansen S and Deriziotis P and Faivre L and Thevenon J and Assoum M and Shriberg L and Kleefstra T and Brunner HG and Wade PA and Fisher SE and Campeau PM},
  year = {2019},
  journal = {Nature communications},
  doi = {10.1038/s41467-019-10161-9},
  url = {https://doi.org/10.1038/s41467-019-10161-9}
}

RIS

TY  - JOUR
TI  - Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
AU  - Snijders Blok L
AU  - Rousseau J
AU  - Twist J
AU  - Ehresmann S
AU  - Takaku M
AU  - Venselaar H
AU  - Rodan LH
AU  - Nowak CB
AU  - Douglas J
AU  - Swoboda KJ
AU  - Steeves MA
AU  - Sahai I
AU  - Stumpel CTRM
AU  - Stegmann APA
AU  - Wheeler P
AU  - Willing M
AU  - Fiala E
AU  - Kochhar A
AU  - Gibson WT
AU  - Cohen ASA
AU  - Agbahovbe R
AU  - Innes AM
AU  - Au PYB
AU  - Rankin J
AU  - Anderson IJ
AU  - Skinner SA
AU  - Louie RJ
AU  - Warren HE
AU  - Afenjar A
AU  - Keren B
AU  - Nava C
AU  - Buratti J
AU  - Isapof A
AU  - Rodriguez D
AU  - Lewandowski R
AU  - Propst J
AU  - van Essen T
AU  - Choi M
AU  - Lee S
AU  - Chae JH
AU  - Price S
AU  - Schnur RE
AU  - Douglas G
AU  - Wentzensen IM
AU  - Zweier C
AU  - Reis A
AU  - Bialer MG
AU  - Moore C
AU  - Koopmans M
AU  - Brilstra EH
AU  - Monroe GR
AU  - van Gassen KLI
AU  - van Binsbergen E
AU  - Newbury-Ecob R
AU  - Bownass L
AU  - Bader I
AU  - Mayr JA
AU  - Wortmann SB
AU  - Jakielski KJ
AU  - Strand EA
AU  - Kloth K
AU  - Bierhals T
AU  - DDD study
AU  - Roberts JD
AU  - Petrovich RM
AU  - Machida S
AU  - Kurumizaka H
AU  - Lelieveld S
AU  - Pfundt R
AU  - Jansen S
AU  - Deriziotis P
AU  - Faivre L
AU  - Thevenon J
AU  - Assoum M
AU  - Shriberg L
AU  - Kleefstra T
AU  - Brunner HG
AU  - Wade PA
AU  - Fisher SE
AU  - Campeau PM
PY  - 2019
JO  - Nature communications
DO  - 10.1038/s41467-019-10161-9
UR  - https://doi.org/10.1038/s41467-019-10161-9
ER  -

APA

L, S. B., J, R., J, T., S, E., M, T., H, V., LH, R., CB, N., J, D., KJ, S., MA, S., I, S., CTRM, S., APA, S., P, W., M, W., E, F., A, K., WT, G., ASA, C., R, A., AM, I., PYB, A., J, R., IJ, A., SA, S., RJ, L., HE, W., A, A., B, K., C, N., J, B., A, I., D, R., R, L., J, P., T, V. E., M, C., S, L., JH, C., S, P., RE, S., G, D., IM, W., C, Z., A, R., MG, B., C, M., M, K., EH, B., GR, M., KLI, V. G., E, V. B., R, N., L, B., I, B., JA, M., SB, W., KJ, J., EA, S., K, K., T, B., study, D., JD, R., RM, P., S, M., H, K., S, L., R, P., S, J., P, D., L, F., J, T., M, A., L, S., T, K., HG, B., PA, W., SE, F., & PM, C. (2019). Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.. Nature communications. https://doi.org/10.1038/s41467-019-10161-9

Source records

pubmed · retrieved 2026-09-26T12:10:25.085Z
europe-pmc · retrieved 2026-09-26T12:10:25.083Z
doaj · retrieved 2026-09-26T12:10:25.061Z