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)

Care4Rare Canada Consortium

doi: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)

Care4Rare Canada Consortium

Research output: Contribution to journal › Comment/Letter to the editor › Academic

1 Citation (Scopus)

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
Pages (from-to)	796
Number of pages	1
Journal	Genetics in medicine
Volume	23
Issue number	4
Early online date	2021
DOIs	https://doi.org/10.1038/s41436-020-01090-w
Publication status	Published - Apr 2021

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https://doi.org/10.1038/s41436-020-01090-w

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@article{3e7cb2313ca842f38cce9bd33256ce88,

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 = "{Care4Rare Canada Consortium} and 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 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 {Van Ziffle}, Jessica",

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

year = "2021",

month = apr,

doi = "https://doi.org/10.1038/s41436-020-01090-w",

language = "English",

volume = "23",

pages = "796",

journal = "Genetics in medicine",

issn = "1098-3600",

publisher = "Lippincott Williams and Wilkins",

number = "4",

}

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 - Care4Rare Canada Consortium

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 - 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 - Van Ziffle, Jessica

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.

UR - http://www.scopus.com/inward/record.url?scp=85102197508&partnerID=8YFLogxK

U2 - https://doi.org/10.1038/s41436-020-01090-w

DO - https://doi.org/10.1038/s41436-020-01090-w

M3 - Comment/Letter to the editor

C2 - 33686260

SN - 1098-3600

VL - 23

SP - 796

JO - Genetics in medicine

JF - Genetics in medicine

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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