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

doi:10.1016/j.ajhg.2019.02.015

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

Research output: Contribution to journal › Comment/debate › peer-review

5 Scopus citations

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.

Original language	English (US)
Pages (from-to)	562
Number of pages	1
Journal	American journal of human genetics
Volume	104
Issue number	3
DOIs	https://doi.org/10.1016/j.ajhg.2019.02.015
State	Published - Mar 7 2019

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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Task Force for Neonatal Genomics, & Deciphering Developmental Disorders Study (2019). 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)). American journal of human genetics, 104(3), 562. https://doi.org/10.1016/j.ajhg.2019.02.015

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.
In: American journal of human genetics, Vol. 104, No. 3, 07.03.2019, p. 562.

Research output: Contribution to journal › Comment/debate › peer-review

Task Force for Neonatal Genomics & Deciphering Developmental Disorders Study 2019, '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))', American journal of human genetics, vol. 104, no. 3, pp. 562. https://doi.org/10.1016/j.ajhg.2019.02.015

Task Force for Neonatal Genomics, Deciphering Developmental Disorders Study. 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)). American journal of human genetics. 2019 Mar 7;104(3):562. doi: 10.1016/j.ajhg.2019.02.015

Task Force for Neonatal Genomics ; Deciphering Developmental Disorders Study. / 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)). In: American journal of human genetics. 2019 ; Vol. 104, No. 3. pp. 562.

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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 Cascino, {Gregory D.}",

note = "Publisher Copyright: {\textcopyright} 2018 American Society of Human Genetics",

year = "2019",

month = mar,

day = "7",

doi = "10.1016/j.ajhg.2019.02.015",

language = "English (US)",

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T2 - 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))

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 - Cascino, Gregory D.

PY - 2019/3/7

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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.

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SP - 562

JO - American journal of human genetics

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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))

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