Correction: De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder (vol 101, pg 716, 2017)

DDD Study; C4RCD Res Grp

doi:10.1016/j.ajhg.2017.12.016

Correction: De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder (vol 101, pg 716, 2017)

DDD Study
, C4RCD Res Grp

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

Abstract

(The American Journal of Human Genetics 101, 716–724; November 2, 2017) The name of author Margot R.F. Reijnders was misspelled in the originally published version of this paper but appears correctly here and has been corrected in the paper online. The authors regret the error.

Original language	English
Pages (from-to)	196-196
Number of pages	1
Journal	American Journal of Human Genetics
Volume	102
Issue number	1
DOIs	https://doi.org/10.1016/j.ajhg.2017.12.016
Publication status	Published - 4 Jan 2018

Access to Document

10.1016/j.ajhg.2017.12.016Licence: Free access - publisher

1 Article

De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder
Lessel, D., Schob, C., Kuery, S., Reinders, M. R. F., Harel, T., Eldomery, M. K., Coban-Akdemir, Z., Denecke, J., Edvardson, S., Colin, E., Stegmann, A. P. A., Gerkes, E. H., Tessarech, M., Bonneau, D., Barth, M., Besnard, T., Cogne, B., Revah-Politi, A., Strom, T. M. & Rosenfeld, J. A. & 24 others, Yang, Y., Posey, J. E., Immken, L., Oundjian, N., Helbig, K. L., Meeks, N., Zegar, K., Morton, J., Schieving, J. H., Claasen, A., Huentelman, M., Narayanan, V., Ramsey, K., Brunner, H. G., Elpeleg, O., Mercier, S., Bezieau, S., Kubisch, C., Kleefstra, T., Kindler, S., Lupski, J. R., Kreienkamp, H.-J., DDD Study & C4RCD Res Grp, 2 Nov 2017, In: American Journal of Human Genetics. 101, 5, p. 716-724 9 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

Cite this

@article{fff1203f16094fbc8e54415799d23f99,

title = "Correction: De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder (vol 101, pg 716, 2017)",

abstract = "(The American Journal of Human Genetics 101, 716{\textendash}724; November 2, 2017) The name of author Margot R.F. Reijnders was misspelled in the originally published version of this paper but appears correctly here and has been corrected in the paper online. The authors regret the error.",

author = "Davor Lessel and Claudia Schob and Sebastien Kury and Reijnders, \{Margot R. F.\} and Tamar Harel and Eldomery, \{Mohammad K.\} and Zeynep Coban-Akdemir and Jonas Denecke and Shimon Edvardson and Estelle Colin and Stegmann, \{Alexander P. A.\} and Gerkes, \{Erica H.\} and Marine Tessarech and Dominique Bonneau and Magalie Barth and Thomas Besnard and Benjamin Cogne and Anya Revah-Politi and Strom, \{Tim M.\} and Rosenfeld, \{Jill A.\} and Yaping Yang and Posey, \{Jennifer E.\} and LaDonna Immken and Nelly Oundjian and Helbig, \{Katherine L.\} and Naomi Meeks and Kelsey Zegar and Jenny Morton and Schieving, \{Jolanda H.\} and Ana Claasen and Matthew Huentelman and Vinodh Narayanan and Keri Ramsey and Brunner, \{Han G.\} and Orly Elpeleg and Sandra Mercier and Stephane Bezieau and Christian Kubisch and Tjitske Kleefstra and Stefan Kindler and Lupski, \{James R.\} and Hans-Jurgen Kreienkamp and \{DDD Study\} and \{C4RCD Res Grp\}",

year = "2018",

month = jan,

day = "4",

doi = "10.1016/j.ajhg.2017.12.016",

language = "English",

volume = "102",

pages = "196--196",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "1",

}

TY - JOUR

T1 - Correction: De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder (vol 101, pg 716, 2017)

AU - Lessel, Davor

AU - Schob, Claudia

AU - Kury, Sebastien

AU - Reijnders, Margot R. F.

AU - Harel, Tamar

AU - Eldomery, Mohammad K.

AU - Coban-Akdemir, Zeynep

AU - Denecke, Jonas

AU - Edvardson, Shimon

AU - Colin, Estelle

AU - Stegmann, Alexander P. A.

AU - Gerkes, Erica H.

AU - Tessarech, Marine

AU - Bonneau, Dominique

AU - Barth, Magalie

AU - Besnard, Thomas

AU - Cogne, Benjamin

AU - Revah-Politi, Anya

AU - Strom, Tim M.

AU - Rosenfeld, Jill A.

AU - Yang, Yaping

AU - Posey, Jennifer E.

AU - Immken, LaDonna

AU - Oundjian, Nelly

AU - Helbig, Katherine L.

AU - Meeks, Naomi

AU - Zegar, Kelsey

AU - Morton, Jenny

AU - Schieving, Jolanda H.

AU - Claasen, Ana

AU - Huentelman, Matthew

AU - Narayanan, Vinodh

AU - Ramsey, Keri

AU - Brunner, Han G.

AU - Elpeleg, Orly

AU - Mercier, Sandra

AU - Bezieau, Stephane

AU - Kubisch, Christian

AU - Kleefstra, Tjitske

AU - Kindler, Stefan

AU - Lupski, James R.

AU - Kreienkamp, Hans-Jurgen

AU - DDD Study

AU - C4RCD Res Grp

PY - 2018/1/4

Y1 - 2018/1/4

N2 - (The American Journal of Human Genetics 101, 716–724; November 2, 2017) The name of author Margot R.F. Reijnders was misspelled in the originally published version of this paper but appears correctly here and has been corrected in the paper online. The authors regret the error.

AB - (The American Journal of Human Genetics 101, 716–724; November 2, 2017) The name of author Margot R.F. Reijnders was misspelled in the originally published version of this paper but appears correctly here and has been corrected in the paper online. The authors regret the error.

U2 - 10.1016/j.ajhg.2017.12.016

DO - 10.1016/j.ajhg.2017.12.016

M3 - Erratum / corrigendum

C2 - 29304375

SN - 0002-9297

VL - 102

SP - 196

EP - 196

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 1

ER -

Correction: De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder (vol 101, pg 716, 2017)

Abstract

Access to Document

Fingerprint

Research output

De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder

Cite this