Erratum: De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias (The American Journal of Human Genetics (2018) 103(5) (666–678), (S0002929718303173), (10.1016/j.ajhg.2018.09.006))

Task Force for Neonatal Genomics, Deciphering Developmental Disorders Study, Katherine L. Helbig, Robert J. Lauerer, Jacqueline C. Bahr, Ivana A. Souza, Candace T. Myers, Betül Uysal, Niklas Schwarz, Maria A. Gandini, Sun Huang, Boris Keren, Cyril Mignot, Alexandra Afenjar, Thierry Billette de Villemeur, Delphine Héron, Caroline Nava, Stéphanie Valence, Julien Buratti, Christina R. Fagerberg & 32 others Kristina P. Soerensen, Maria Kibaek, Erik Jan Kamsteeg, David A. Koolen, Boudewijn Gunning, H. Jurgen Schelhaas, Michael C. Kruer, Jordana Fox, Somayeh Bakhtiari, Randa Jarrar, Sergio Padilla-Lopez, Kristin Lindstrom, Sheng Chih Jin, Xue Zeng, Kaya Bilguvar, Antigone Papavasileiou, Qinghe Xing, Changlian Zhu, Katja Boysen, Filippo Vairo, Brendan C. Lanpher, Eric W. Klee, Jan Mendelt Tillema, Eric T. Payne, Margot A. Cousin, Teresa M. Kruisselbrink, Myra J. Wick, Joshua Baker, Eric Haan, Nicholas Smith, Azita Sadeghpour, Jozef Gecz

Research output: Contribution to journalComment/debate

Abstract

(The American Journal of Human Genetics 103, 666–678; November 1, 2018) In the version of this article originally published online, Qinghe Xing's name was misspelled as Qinghe Xin. Also, Azita Sadeghpour, Erica E. Davis, and Nicholas Katsanis (all at Center for Human Disease Modeling, Duke University Medical Center, Durham, NC 27701, USA) and the Task Force for Neonatal Genomics were omitted from the author list. The members of the Task Force for Neonatal Genomics are as follows: Alexander Allori, Misha Angrist, Patricia Ashley, Margarita Bidegain, Brita Boyd, Eileen Chambers, Heidi Cope, C. Michael Cotten, Theresa Curington, Erica E. Davis, Sarah Ellestad, Kimberley Fisher, Amanda French, William Gallentine, Ronald Goldberg, Kevin Hill, Sujay Kansagra, Nicholas Katsanis, Sara Katsanis, Joanne Kurtzberg, Jeffrey Marcus, Marie McDonald, Mohammed Mikati, Stephen Miller, Amy Murtha, Yezmin Perilla, Carolyn Pizoli, Todd Purves, Sherry Ross, Azita Sadeghpour, Edward Smith, and John Wiener. The authors apologize for these omissions.

LanguageEnglish
Number of pages1
JournalAmerican Journal of Human Genetics
Volume104
Issue number3
DOIs
Publication statusPublished - 7 Mar 2019

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

@article{bde1ff32c78246f091cb6a4d7b5a0173,
title = "Erratum: De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias (The American Journal of Human Genetics (2018) 103(5) (666–678), (S0002929718303173), (10.1016/j.ajhg.2018.09.006))",
abstract = "(The American Journal of Human Genetics 103, 666–678; November 1, 2018) In the version of this article originally published online, Qinghe Xing's name was misspelled as Qinghe Xin. Also, Azita Sadeghpour, Erica E. Davis, and Nicholas Katsanis (all at Center for Human Disease Modeling, Duke University Medical Center, Durham, NC 27701, USA) and the Task Force for Neonatal Genomics were omitted from the author list. The members of the Task Force for Neonatal Genomics are as follows: Alexander Allori, Misha Angrist, Patricia Ashley, Margarita Bidegain, Brita Boyd, Eileen Chambers, Heidi Cope, C. Michael Cotten, Theresa Curington, Erica E. Davis, Sarah Ellestad, Kimberley Fisher, Amanda French, William Gallentine, Ronald Goldberg, Kevin Hill, Sujay Kansagra, Nicholas Katsanis, Sara Katsanis, Joanne Kurtzberg, Jeffrey Marcus, Marie McDonald, Mohammed Mikati, Stephen Miller, Amy Murtha, Yezmin Perilla, Carolyn Pizoli, Todd Purves, Sherry Ross, Azita Sadeghpour, Edward Smith, and John Wiener. The authors apologize for these omissions.",
author = "{Task Force for Neonatal Genomics} and {Deciphering Developmental Disorders Study} and Helbig, {Katherine L.} and Lauerer, {Robert J.} and Bahr, {Jacqueline C.} and Souza, {Ivana A.} and Myers, {Candace T.} and Bet{\"u}l Uysal and Niklas Schwarz and Gandini, {Maria A.} and Sun Huang and Boris Keren and Cyril Mignot and Alexandra Afenjar and {Billette de Villemeur}, Thierry and Delphine H{\'e}ron and Caroline Nava and St{\'e}phanie Valence and Julien Buratti and Fagerberg, {Christina R.} and Soerensen, {Kristina P.} and Maria Kibaek and Kamsteeg, {Erik Jan} and Koolen, {David A.} and Boudewijn Gunning and Schelhaas, {H. Jurgen} and Kruer, {Michael C.} and Jordana Fox and Somayeh Bakhtiari and Randa Jarrar and Sergio Padilla-Lopez and Kristin Lindstrom and Jin, {Sheng Chih} and Xue Zeng and Kaya Bilguvar and Antigone Papavasileiou and Qinghe Xing and Changlian Zhu and Katja Boysen and Filippo Vairo and Lanpher, {Brendan C.} and Klee, {Eric W.} and Tillema, {Jan Mendelt} and Payne, {Eric T.} and Cousin, {Margot A.} and Kruisselbrink, {Teresa M.} and Wick, {Myra J.} and Joshua Baker and Eric Haan and Nicholas Smith and Azita Sadeghpour and Jozef Gecz",
year = "2019",
month = "3",
day = "7",
doi = "10.1016/j.ajhg.2019.02.015",
language = "English",
volume = "104",
journal = "American Journal of Human Genetics",
issn = "0002-9297",
publisher = "Cell Press",
number = "3",

}

TY - JOUR

T1 - Erratum

T2 - American Journal of Human Genetics

AU - Task Force for Neonatal Genomics

AU - Deciphering Developmental Disorders Study

AU - Helbig, Katherine L.

AU - Lauerer, Robert J.

AU - Bahr, Jacqueline C.

AU - Souza, Ivana A.

AU - Myers, Candace T.

AU - Uysal, Betül

AU - Schwarz, Niklas

AU - Gandini, Maria A.

AU - Huang, Sun

AU - Keren, Boris

AU - Mignot, Cyril

AU - Afenjar, Alexandra

AU - Billette de Villemeur, Thierry

AU - Héron, Delphine

AU - Nava, Caroline

AU - Valence, Stéphanie

AU - Buratti, Julien

AU - Fagerberg, Christina R.

AU - Soerensen, Kristina P.

AU - Kibaek, Maria

AU - Kamsteeg, Erik Jan

AU - Koolen, David A.

AU - Gunning, Boudewijn

AU - Schelhaas, H. Jurgen

AU - Kruer, Michael C.

AU - Fox, Jordana

AU - Bakhtiari, Somayeh

AU - Jarrar, Randa

AU - Padilla-Lopez, Sergio

AU - Lindstrom, Kristin

AU - Jin, Sheng Chih

AU - Zeng, Xue

AU - Bilguvar, Kaya

AU - Papavasileiou, Antigone

AU - Xing, Qinghe

AU - Zhu, Changlian

AU - Boysen, Katja

AU - Vairo, Filippo

AU - Lanpher, Brendan C.

AU - Klee, Eric W.

AU - Tillema, Jan Mendelt

AU - Payne, Eric T.

AU - Cousin, Margot A.

AU - Kruisselbrink, Teresa M.

AU - Wick, Myra J.

AU - Baker, Joshua

AU - Haan, Eric

AU - Smith, Nicholas

AU - Sadeghpour, Azita

AU - Gecz, Jozef

PY - 2019/3/7

Y1 - 2019/3/7

N2 - (The American Journal of Human Genetics 103, 666–678; November 1, 2018) In the version of this article originally published online, Qinghe Xing's name was misspelled as Qinghe Xin. Also, Azita Sadeghpour, Erica E. Davis, and Nicholas Katsanis (all at Center for Human Disease Modeling, Duke University Medical Center, Durham, NC 27701, USA) and the Task Force for Neonatal Genomics were omitted from the author list. The members of the Task Force for Neonatal Genomics are as follows: Alexander Allori, Misha Angrist, Patricia Ashley, Margarita Bidegain, Brita Boyd, Eileen Chambers, Heidi Cope, C. Michael Cotten, Theresa Curington, Erica E. Davis, Sarah Ellestad, Kimberley Fisher, Amanda French, William Gallentine, Ronald Goldberg, Kevin Hill, Sujay Kansagra, Nicholas Katsanis, Sara Katsanis, Joanne Kurtzberg, Jeffrey Marcus, Marie McDonald, Mohammed Mikati, Stephen Miller, Amy Murtha, Yezmin Perilla, Carolyn Pizoli, Todd Purves, Sherry Ross, Azita Sadeghpour, Edward Smith, and John Wiener. The authors apologize for these omissions.

AB - (The American Journal of Human Genetics 103, 666–678; November 1, 2018) In the version of this article originally published online, Qinghe Xing's name was misspelled as Qinghe Xin. Also, Azita Sadeghpour, Erica E. Davis, and Nicholas Katsanis (all at Center for Human Disease Modeling, Duke University Medical Center, Durham, NC 27701, USA) and the Task Force for Neonatal Genomics were omitted from the author list. The members of the Task Force for Neonatal Genomics are as follows: Alexander Allori, Misha Angrist, Patricia Ashley, Margarita Bidegain, Brita Boyd, Eileen Chambers, Heidi Cope, C. Michael Cotten, Theresa Curington, Erica E. Davis, Sarah Ellestad, Kimberley Fisher, Amanda French, William Gallentine, Ronald Goldberg, Kevin Hill, Sujay Kansagra, Nicholas Katsanis, Sara Katsanis, Joanne Kurtzberg, Jeffrey Marcus, Marie McDonald, Mohammed Mikati, Stephen Miller, Amy Murtha, Yezmin Perilla, Carolyn Pizoli, Todd Purves, Sherry Ross, Azita Sadeghpour, Edward Smith, and John Wiener. The authors apologize for these omissions.

UR - http://www.scopus.com/inward/record.url?scp=85061871052&partnerID=8YFLogxK

U2 - 10.1016/j.ajhg.2019.02.015

DO - 10.1016/j.ajhg.2019.02.015

M3 - Comment/debate

VL - 104

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

SN - 0002-9297

IS - 3

ER -