Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (Genetics in Medicine, (2021), 23, 4, (653-660), 10.1038/s41436-020-01020-w)

Chiara Klöckner; Heinrich Sticht; Pia Zacher; Bernt Popp; Holly E. Babcock; Dewi P. Bakker; Katy Barwick; Michaela V. Bonfert; Carsten G. Bönnemann; Eva H. Brilstra; Care4Rare Canada Consortium; Wendy K. Chung; Angus J. Clarke; Patrick Devine; Sandra Donkervoort; Jamie L. Fraser; Jennifer Friedman; Alyssa Gates; Jamal Ghoumid; Emma Hobson; Gabriella Horvath; Jennifer Keller-Ramey; Boris Keren; Manju A. Kurian; Virgina Lee; Kathleen A. Leppig; Johan Lundgren; Marie T. McDonald; Heather M. McLaughlin; Amy McTague; Heather C. Mefford; Cyril Mignot; Mohamad A. Mikati; Caroline Nava; F. Lucy Raymond; Julian R. Sampson; Alba Sanchis-Juan; Vandana Shashi; Joseph T.C. Shieh; Marwan Shinawi; Anne Slavotinek; Tommy Stödberg; Nicholas Stong; Jennifer A. Sullivan; Ashley C. Taylor; Tomi L. Toler; Marie José van den Boogaard; Saskia N. van der Crabben; Koen L.I. van Gassen; Richard H. van Jaarsveld; Rikke S. Møller; Johannes W Lemke; Konrad Platzer

doi:10.1038/s41436-020-01090-w

Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (Genetics in Medicine, (2021), 23, 4, (653-660), 10.1038/s41436-020-01020-w)

Chiara Klöckner, Heinrich Sticht, Pia Zacher, Bernt Popp, Holly E. Babcock, Dewi P. Bakker, Katy Barwick, Michaela V. Bonfert, Carsten G. Bönnemann, Eva H. Brilstra, Care4Rare Canada Consortium, Wendy K. Chung, Angus J. Clarke, Patrick Devine, Sandra Donkervoort, Jamie L. Fraser, Jennifer Friedman, Alyssa Gates, Jamal Ghoumid, Emma HobsonGabriella Horvath, Jennifer Keller-Ramey, Boris Keren, Manju A. Kurian, Virgina Lee, Kathleen A. Leppig, Johan Lundgren, Marie T. McDonald, Heather M. McLaughlin, Amy McTague, Heather C. Mefford, Cyril Mignot, Mohamad A. Mikati, Caroline Nava, F. Lucy Raymond, Julian R. Sampson, Alba Sanchis-Juan, Vandana Shashi, Joseph T.C. Shieh, Marwan Shinawi, Anne Slavotinek, Tommy Stödberg, Nicholas Stong, Jennifer A. Sullivan, Ashley C. Taylor, Tomi L. Toler, Marie José van den Boogaard, Saskia N. van der Crabben, Koen L.I. van Gassen, Richard H. van Jaarsveld, Rikke S. Møller, Johannes W Lemke, Konrad Platzer

IRS - The Epilepsyhospital Filadelfia, Research Unit of Epilepsy Genetics and Personalized Medicine (Dianalund)

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

Abstract

Unfortunately, in the first sentence in the abstract, a spelling mistake was introduced during the production process after our proofreading. The wording was changed from “aims” to “aimsed.” Heather M. McLaughlin was not listed among the authors. The original article has been corrected.

Original language	English
Journal	Genetics in Medicine
Volume	23
Issue number	4
Pages (from-to)	796
ISSN	1098-3600
DOIs	https://doi.org/10.1038/s41436-020-01090-w
Publication status	Published - Apr 2021

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10.1038/s41436-020-01090-w

Cite this

Klöckner, C., Sticht, H., Zacher, P., Popp, B., Babcock, H. E., Bakker, D. P., Barwick, K., Bonfert, M. V., Bönnemann, C. G., Brilstra, E. H., Care4Rare Canada Consortium, Chung, W. K., Clarke, A. J., Devine, P., Donkervoort, S., Fraser, J. L., Friedman, J., Gates, A., Ghoumid, J., ... Platzer, K. (2021). Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (Genetics in Medicine, (2021), 23, 4, (653-660), 10.1038/s41436-020-01020-w). Genetics in Medicine, 23(4), 796. https://doi.org/10.1038/s41436-020-01090-w

Klöckner, Chiara ; Sticht, Heinrich ; Zacher, Pia ; Popp, Bernt ; Babcock, Holly E. ; Bakker, Dewi P. ; Barwick, Katy ; Bonfert, Michaela V. ; Bönnemann, Carsten G. ; Brilstra, Eva H. ; Care4Rare Canada Consortium ; Chung, Wendy K. ; Clarke, Angus J. ; Devine, Patrick ; Donkervoort, Sandra ; Fraser, Jamie L. ; Friedman, Jennifer ; Gates, Alyssa ; Ghoumid, Jamal ; Hobson, Emma ; Horvath, Gabriella ; Keller-Ramey, Jennifer ; Keren, Boris ; Kurian, Manju A. ; Lee, Virgina ; Leppig, Kathleen A. ; Lundgren, Johan ; McDonald, Marie T. ; McLaughlin, Heather M. ; McTague, Amy ; Mefford, Heather C. ; Mignot, Cyril ; Mikati, Mohamad A. ; Nava, Caroline ; Raymond, F. Lucy ; Sampson, Julian R. ; Sanchis-Juan, Alba ; Shashi, Vandana ; Shieh, Joseph T.C. ; Shinawi, Marwan ; Slavotinek, Anne ; Stödberg, Tommy ; Stong, Nicholas ; Sullivan, Jennifer A. ; Taylor, Ashley C. ; Toler, Tomi L. ; van den Boogaard, Marie José ; van der Crabben, Saskia N. ; van Gassen, Koen L.I. ; van Jaarsveld, Richard H. ; Møller, Rikke S. ; Lemke, Johannes W ; Platzer, Konrad. / Correction to : De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (Genetics in Medicine, (2021), 23, 4, (653-660), 10.1038/s41436-020-01020-w). In: Genetics in Medicine. 2021 ; Vol. 23, No. 4. pp. 796.

@article{376ef31d36c34940b89891de4fb86135,

title = "Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (Genetics in Medicine, (2021), 23, 4, (653-660), 10.1038/s41436-020-01020-w)",

abstract = "Unfortunately, in the first sentence in the abstract, a spelling mistake was introduced during the production process after our proofreading. The wording was changed from “aims” to “aimsed.” Heather M. McLaughlin was not listed among the authors. The original article has been corrected.",

author = "Chiara Kl{\"o}ckner and Heinrich Sticht and Pia Zacher and Bernt Popp and Babcock, {Holly E.} and Bakker, {Dewi P.} and Katy Barwick and Bonfert, {Michaela V.} and B{\"o}nnemann, {Carsten G.} and Brilstra, {Eva H.} and {Care4Rare Canada Consortium} and Chung, {Wendy K.} and Clarke, {Angus J.} and Patrick Devine and Sandra Donkervoort and Fraser, {Jamie L.} and Jennifer Friedman and Alyssa Gates and Jamal Ghoumid and Emma Hobson and Gabriella Horvath and Jennifer Keller-Ramey and Boris Keren and Kurian, {Manju A.} and Virgina Lee and Leppig, {Kathleen A.} and Johan Lundgren and McDonald, {Marie T.} and McLaughlin, {Heather M.} and Amy McTague and Mefford, {Heather C.} and Cyril Mignot and Mikati, {Mohamad A.} and Caroline Nava and Raymond, {F. Lucy} and Sampson, {Julian R.} and Alba Sanchis-Juan and Vandana Shashi and Shieh, {Joseph T.C.} and Marwan Shinawi and Anne Slavotinek and Tommy St{\"o}dberg and Nicholas Stong and Sullivan, {Jennifer A.} and Taylor, {Ashley C.} and Toler, {Tomi L.} and {van den Boogaard}, {Marie Jos{\'e}} and {van der Crabben}, {Saskia N.} and {van Gassen}, {Koen L.I.} and {van Jaarsveld}, {Richard H.} and M{\o}ller, {Rikke S.} and Lemke, {Johannes W} and Konrad Platzer",

note = "Publisher Copyright: {\textcopyright} 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.",

year = "2021",

month = apr,

doi = "10.1038/s41436-020-01090-w",

language = "English",

volume = "23",

pages = "796",

journal = "Genetics in Medicine",

issn = "1098-3600",

publisher = "Nature Publishing Group",

number = "4",

}

Klöckner, C, Sticht, H, Zacher, P, Popp, B, Babcock, HE, Bakker, DP, Barwick, K, Bonfert, MV, Bönnemann, CG, Brilstra, EH, Care4Rare Canada Consortium, Chung, WK, Clarke, AJ, Devine, P, Donkervoort, S, Fraser, JL, Friedman, J, Gates, A, Ghoumid, J, Hobson, E, Horvath, G, Keller-Ramey, J, Keren, B, Kurian, MA, Lee, V, Leppig, KA, Lundgren, J, McDonald, MT, McLaughlin, HM, McTague, A, Mefford, HC, Mignot, C, Mikati, MA, Nava, C, Raymond, FL, Sampson, JR, Sanchis-Juan, A, Shashi, V, Shieh, JTC, Shinawi, M, Slavotinek, A, Stödberg, T, Stong, N, Sullivan, JA, Taylor, AC, Toler, TL, van den Boogaard, MJ, van der Crabben, SN, van Gassen, KLI, van Jaarsveld, RH, Møller, RS, Lemke, JW & Platzer, K 2021, 'Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (Genetics in Medicine, (2021), 23, 4, (653-660), 10.1038/s41436-020-01020-w)', Genetics in Medicine, vol. 23, no. 4, pp. 796. https://doi.org/10.1038/s41436-020-01090-w

Correction to : De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (Genetics in Medicine, (2021), 23, 4, (653-660), 10.1038/s41436-020-01020-w). / Klöckner, Chiara; Sticht, Heinrich; Zacher, Pia; Popp, Bernt; Babcock, Holly E.; Bakker, Dewi P.; Barwick, Katy; Bonfert, Michaela V.; Bönnemann, Carsten G.; Brilstra, Eva H.; Care4Rare Canada Consortium; Chung, Wendy K.; Clarke, Angus J.; Devine, Patrick; Donkervoort, Sandra; Fraser, Jamie L.; Friedman, Jennifer; Gates, Alyssa; Ghoumid, Jamal; Hobson, Emma; Horvath, Gabriella; Keller-Ramey, Jennifer; Keren, Boris; Kurian, Manju A.; Lee, Virgina; Leppig, Kathleen A.; Lundgren, Johan; McDonald, Marie T.; McLaughlin, Heather M.; McTague, Amy; Mefford, Heather C.; Mignot, Cyril; Mikati, Mohamad A.; Nava, Caroline; Raymond, F. Lucy; Sampson, Julian R.; Sanchis-Juan, Alba; Shashi, Vandana; Shieh, Joseph T.C.; Shinawi, Marwan; Slavotinek, Anne; Stödberg, Tommy; Stong, Nicholas; Sullivan, Jennifer A.; Taylor, Ashley C.; Toler, Tomi L.; van den Boogaard, Marie José; van der Crabben, Saskia N.; van Gassen, Koen L.I.; van Jaarsveld, Richard H.; Møller, Rikke S.; Lemke, Johannes W; Platzer, Konrad.

In: Genetics in Medicine, Vol. 23, No. 4, 04.2021, p. 796.

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

TY - JOUR

T1 - Correction to

T2 - De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (Genetics in Medicine, (2021), 23, 4, (653-660), 10.1038/s41436-020-01020-w)

AU - Klöckner, Chiara

AU - Sticht, Heinrich

AU - Zacher, Pia

AU - Popp, Bernt

AU - Babcock, Holly E.

AU - Bakker, Dewi P.

AU - Barwick, Katy

AU - Bonfert, Michaela V.

AU - Bönnemann, Carsten G.

AU - Brilstra, Eva H.

AU - Care4Rare Canada Consortium

AU - Chung, Wendy K.

AU - Clarke, Angus J.

AU - Devine, Patrick

AU - Donkervoort, Sandra

AU - Fraser, Jamie L.

AU - Friedman, Jennifer

AU - Gates, Alyssa

AU - Ghoumid, Jamal

AU - Hobson, Emma

AU - Horvath, Gabriella

AU - Keller-Ramey, Jennifer

AU - Keren, Boris

AU - Kurian, Manju A.

AU - Lee, Virgina

AU - Leppig, Kathleen A.

AU - Lundgren, Johan

AU - McDonald, Marie T.

AU - McLaughlin, Heather M.

AU - McTague, Amy

AU - Mefford, Heather C.

AU - Mignot, Cyril

AU - Mikati, Mohamad A.

AU - Nava, Caroline

AU - Raymond, F. Lucy

AU - Sampson, Julian R.

AU - Sanchis-Juan, Alba

AU - Shashi, Vandana

AU - Shieh, Joseph T.C.

AU - Shinawi, Marwan

AU - Slavotinek, Anne

AU - Stödberg, Tommy

AU - Stong, Nicholas

AU - Sullivan, Jennifer A.

AU - Taylor, Ashley C.

AU - Toler, Tomi L.

AU - van den Boogaard, Marie José

AU - van der Crabben, Saskia N.

AU - van Gassen, Koen L.I.

AU - van Jaarsveld, Richard H.

AU - Møller, Rikke S.

AU - Lemke, Johannes W

AU - Platzer, Konrad

PY - 2021/4

Y1 - 2021/4

N2 - Unfortunately, in the first sentence in the abstract, a spelling mistake was introduced during the production process after our proofreading. The wording was changed from “aims” to “aimsed.” Heather M. McLaughlin was not listed among the authors. The original article has been corrected.

AB - Unfortunately, in the first sentence in the abstract, a spelling mistake was introduced during the production process after our proofreading. The wording was changed from “aims” to “aimsed.” Heather M. McLaughlin was not listed among the authors. The original article has been corrected.

U2 - 10.1038/s41436-020-01090-w

DO - 10.1038/s41436-020-01090-w

M3 - Comment/debate

C2 - 33686260

AN - SCOPUS:85102197508

VL - 23

SP - 796

JO - Genetics in Medicine

JF - Genetics in Medicine

SN - 1098-3600

IS - 4

ER -

Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (Genetics in Medicine, (2021), 23, 4, (653-660), 10.1038/s41436-020-01020-w)

Abstract

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