Erratum: De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder (The American Journal of Human Genetics (2017) 101(5) (716–724)(S000292971730383X)(10.1016/j.ajhg.2017.09.014))

C4RCD Research Group

doi:10.1016/j.ajhg.2017.12.016

Erratum: De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder (The American Journal of Human Genetics (2017) 101(5) (716–724)(S000292971730383X)(10.1016/j.ajhg.2017.09.014))

C4RCD Research Group

Faculty of Health Sciences

Research output: Contribution to journal › Comment/debate

6 Scopus citations

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
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
State	Published - 4 Jan 2018

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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@article{903203e4bb3647ee890ff31302506d78,

title = "Erratum: De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder (The American Journal of Human Genetics (2017) 101(5) (716–724)(S000292971730383X)(10.1016/j.ajhg.2017.09.014))",

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.",

author = "{C4RCD Research Group} and Davor Lessel and Claudia Schob and S{\'e}bastien K{\"u}ry 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 Cogn{\'e} and Anya Revah-Politi and Strom, {Tim M.} and Rosenfeld, {Jill A.} and Yaping Yang and Posey, {Jennifer E.} and Immken, {La Donna} and Nelly Oundjian and Helbig, {Katherine L.} and Naomi Meeks and Kelsey Zegar and Jenny Morton and {the DDD study}, {DDD study} 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 St{\'e}phane B{\'e}zieau and Christian Kubisch and Tjitske Kleefstra and Stefan Kindler and Lupski, {James R.} and Kreienkamp, {Hans J{\"u}rgen}",

note = "Publisher Copyright: {\textcopyright} 2017 American Society of Human Genetics",

year = "2018",

month = jan,

day = "4",

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

language = "English",

volume = "102",

pages = "196",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "1",

}

Erratum: De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder (The American Journal of Human Genetics (2017) 101(5) (716–724)(S000292971730383X)(10.1016/j.ajhg.2017.09.014)). / C4RCD Research Group.
In: American Journal of Human Genetics, Vol. 102, No. 1, 04.01.2018, p. 196.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Erratum

T2 - De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder (The American Journal of Human Genetics (2017) 101(5) (716–724)(S000292971730383X)(10.1016/j.ajhg.2017.09.014))

AU - C4RCD Research Group

AU - Lessel, Davor

AU - Schob, Claudia

AU - Küry, Sébastien

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 - Cogné, Benjamin

AU - Revah-Politi, Anya

AU - Strom, Tim M.

AU - Rosenfeld, Jill A.

AU - Yang, Yaping

AU - Posey, Jennifer E.

AU - Immken, La Donna

AU - Oundjian, Nelly

AU - Helbig, Katherine L.

AU - Meeks, Naomi

AU - Zegar, Kelsey

AU - Morton, Jenny

AU - the DDD study, DDD study

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 - Bézieau, Stéphane

AU - Kubisch, Christian

AU - Kleefstra, Tjitske

AU - Kindler, Stefan

AU - Lupski, James R.

AU - Kreienkamp, Hans Jürgen

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.

UR - http://www.scopus.com/inward/record.url?scp=85039712872&partnerID=8YFLogxK

U2 - 10.1016/j.ajhg.2017.12.016

DO - 10.1016/j.ajhg.2017.12.016

M3 - Comment/debate

C2 - 29304375

AN - SCOPUS:85039712872

SN - 0002-9297

VL - 102

SP - 196

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 1

ER -

Erratum: De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder (The American Journal of Human Genetics (2017) 101(5) (716–724)(S000292971730383X)(10.1016/j.ajhg.2017.09.014))

Abstract

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