Correction: De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias

Deciphering Developmental Disorders Study; Task Force for Neonatal Genomics; KL Helbig; RJ Lauerer; JC Bahr; IA Souza; CT Myers; B Uysal; N Schwarz; MA Gandini; S Huang; B Keren; C Mignot; A Afenjar; de Villemeur T Billette; Delphine Héron; Caroline Nava; Stéphanie Valence; Julien Buratti; Christina R Fagerberg; 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; Bronwyn Kerr; Imelda Hughes; Siddharth Banka

doi:10.1016/j.ajhg.2019.02.015

Correction: De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias

Deciphering Developmental Disorders Study, Task Force for Neonatal Genomics, KL Helbig, RJ Lauerer, JC Bahr, IA Souza, CT Myers, B Uysal, N Schwarz, MA Gandini, S Huang, B Keren, C Mignot, A Afenjar, de Villemeur T Billette, Delphine Héron, Caroline Nava, Stéphanie Valence, Julien Buratti, Christina R FagerbergKristina 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, Bronwyn Kerr, Imelda Hughes, Siddharth Banka

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	P562
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
Publication status	Published - 7 Mar 2019

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10.1016/j.ajhg.2019.02.015

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Deciphering Developmental Disorders Study, Task Force for Neonatal Genomics, Helbig, KL., Lauerer, RJ., Bahr, JC., Souza, IA., Myers, CT., Uysal, B., Schwarz, N., Gandini, MA., Huang, S., Keren, B., Mignot, C., Afenjar, A., Billette, D. V. T., Héron, D., Nava, C., Valence, S., Buratti, J., ... Banka, S. (2019). Correction: De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias. American Journal of Human Genetics, 104(3), P562. https://doi.org/10.1016/j.ajhg.2019.02.015

@article{fc4ac340f5bd47d695f9e21fef427cf9,

title = "Correction: De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias",

author = "{Deciphering Developmental Disorders Study} and {Task Force for Neonatal Genomics} and KL Helbig and RJ Lauerer and JC Bahr and IA Souza and CT Myers and B Uysal and N Schwarz and MA Gandini and S Huang and B Keren and C Mignot and A Afenjar and Billette, {de Villemeur T} 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 Erik-Jan Kamsteeg 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 Jan-Mendelt Tillema and Payne, {Eric T} and Cousin, {Margot A} and Kruisselbrink, {Teresa M} and Wick, {Myra J.} and Joshua Baker and Eric Haan and Bronwyn Kerr and Imelda Hughes and Siddharth Banka",

year = "2019",

month = mar,

day = "7",

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

language = "English",

volume = "104",

pages = "P562",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "3",

}

Deciphering Developmental Disorders Study, Task Force for Neonatal Genomics, Helbig, KL, Lauerer, RJ, Bahr, JC, Souza, IA, Myers, CT, Uysal, B, Schwarz, N, Gandini, MA, Huang, S, Keren, B, Mignot, C, Afenjar, A, Billette, DVT, Héron, D, Nava, C, Valence, S, Buratti, J, Fagerberg, CR, Soerensen, KP, Kibaek, M, Kamsteeg, E-J, Koolen, DA, Gunning, B, Schelhaas, HJ, Kruer, MC, Fox, J, Bakhtiari, S, Jarrar, R, Padilla-Lopez, S, Lindstrom, K, Jin, SC, Zeng, X, Bilguvar, K, Papavasileiou, A, Xing, Q, Zhu, C, Boysen, K, Vairo, F, Lanpher, BC, Klee, EW, Tillema, J-M, Payne, ET, Cousin, MA, Kruisselbrink, TM, Wick, MJ, Baker, J, Haan, E, Kerr, B, Hughes, I & Banka, S 2019, 'Correction: De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias', American Journal of Human Genetics, vol. 104, no. 3, pp. P562. https://doi.org/10.1016/j.ajhg.2019.02.015

Correction: De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias. / Deciphering Developmental Disorders Study; Task Force for Neonatal Genomics; Helbig, KL et al.
In: American Journal of Human Genetics, Vol. 104, No. 3, 07.03.2019, p. P562.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Correction

T2 - De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias

AU - Deciphering Developmental Disorders Study

AU - Task Force for Neonatal Genomics

AU - Helbig, KL

AU - Lauerer, RJ

AU - Bahr, JC

AU - Souza, IA

AU - Myers, CT

AU - Uysal, B

AU - Schwarz, N

AU - Gandini, MA

AU - Huang, S

AU - Keren, B

AU - Mignot, C

AU - Afenjar, A

AU - Billette, de Villemeur T

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 - Kerr, Bronwyn

AU - Hughes, Imelda

AU - Banka, Siddharth

PY - 2019/3/7

Y1 - 2019/3/7

UR - http://europepmc.org/abstract/med/30849329

U2 - 10.1016/j.ajhg.2019.02.015

DO - 10.1016/j.ajhg.2019.02.015

M3 - Article

C2 - 30849329

SN - 0002-9297

VL - 104

SP - P562

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 3

ER -

Correction: De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias

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