Erratum: De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia (The American Journal of Human Genetics (2019) 105(2) (413–424), (S0002929719302393), (10.1016/j.ajhg.2019.06.014))

Undiagnosed Diseases Network

Research output: Contribution to journalComment/debate

Abstract

(The American Journal of Human Genetics 105, 413–424; August 1, 2019) In the originally published version of this article, Figures 3B and 3C included the allele name “sisy” but the correct term is “wrd37,” as appears in the rest of the article. In addition, there are two edits in Figure 3A: Thr125 has been highlighted instead of Thr124 and “Patient variants” has been changed to “Protein variants.” All these changes are reflected in the figure below and in the article online. The authors regret these errors. [Figure presented] [Figure presented]

Original languageEnglish (US)
Pages (from-to)672-674
Number of pages3
JournalAmerican journal of human genetics
Volume105
Issue number3
DOIs
StatePublished - Sep 5 2019

Fingerprint

Coloboma
Medical Genetics
Intellectual Disability
Names
Epilepsy
Emotions
Alleles
Proteins
Cerebellar Hypoplasia

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

@article{242edd64868442f7bfc7e58ac7d64d6c,
title = "Erratum: De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia (The American Journal of Human Genetics (2019) 105(2) (413–424), (S0002929719302393), (10.1016/j.ajhg.2019.06.014))",
abstract = "(The American Journal of Human Genetics 105, 413–424; August 1, 2019) In the originally published version of this article, Figures 3B and 3C included the allele name “sisy” but the correct term is “wrd37,” as appears in the rest of the article. In addition, there are two edits in Figure 3A: Thr125 has been highlighted instead of Thr124 and “Patient variants” has been changed to “Protein variants.” All these changes are reflected in the figure below and in the article online. The authors regret these errors. [Figure presented] [Figure presented]",
author = "{Undiagnosed Diseases Network} and Oguz Kanca and Andrews, {Jonathan C.} and Lee, {Pei Tseng} and Chirag Patel and Braddock, {Stephen R.} and Slavotinek, {Anne M.} and Cohen, {Julie S.} and Gubbels, {Cynthia S.} and Aldinger, {Kimberly A.} and Judy Williams and Maanasa Indaram and Ali Fatemi and Yu, {Timothy W.} and Agrawal, {Pankaj B.} and Gilbert Vezina and Cas Simons and Joanna Crawford and Lau, {C. Christopher} and Acosta, {Maria T.} and Adams, {David R.} and Pankaj Agrawal and Alejandro, {Mercedes E.} and Patrick Allard and Justin Alvey and Ashley Andrews and Ashley, {Euan A.} and Azamian, {Mahshid S.} and Bacino, {Carlos A.} and Guney Bademci and Eva Baker and Ashok Balasubramanyam and Dustin Baldridge and Jim Bale and Deborah Barbouth and Batzli, {Gabriel F.} and Pinar Bayrak-Toydemir and Beggs, {Alan H.} and Gill Bejerano and Bellen, {Hugo J.} and Bernstein, {Jonathan A.} and Berry, {Gerard T.} and Anna Bican and Bick, {David P.} and Birch, {Camille L.} and Stephanie Bivona and John Bohnsack and Lanpher, {Brendan C.} and Lanza, {Ian R.} and Eva Morava-Kozicz and Devin Oglesbee",
year = "2019",
month = "9",
day = "5",
doi = "10.1016/j.ajhg.2019.07.017",
language = "English (US)",
volume = "105",
pages = "672--674",
journal = "American Journal of Human Genetics",
issn = "0002-9297",
publisher = "Cell Press",
number = "3",

}

TY - JOUR

T1 - Erratum

T2 - De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia (The American Journal of Human Genetics (2019) 105(2) (413–424), (S0002929719302393), (10.1016/j.ajhg.2019.06.014))

AU - Undiagnosed Diseases Network

AU - Kanca, Oguz

AU - Andrews, Jonathan C.

AU - Lee, Pei Tseng

AU - Patel, Chirag

AU - Braddock, Stephen R.

AU - Slavotinek, Anne M.

AU - Cohen, Julie S.

AU - Gubbels, Cynthia S.

AU - Aldinger, Kimberly A.

AU - Williams, Judy

AU - Indaram, Maanasa

AU - Fatemi, Ali

AU - Yu, Timothy W.

AU - Agrawal, Pankaj B.

AU - Vezina, Gilbert

AU - Simons, Cas

AU - Crawford, Joanna

AU - Lau, C. Christopher

AU - Acosta, Maria T.

AU - Adams, David R.

AU - Agrawal, Pankaj

AU - Alejandro, Mercedes E.

AU - Allard, Patrick

AU - Alvey, Justin

AU - Andrews, Ashley

AU - Ashley, Euan A.

AU - Azamian, Mahshid S.

AU - Bacino, Carlos A.

AU - Bademci, Guney

AU - Baker, Eva

AU - Balasubramanyam, Ashok

AU - Baldridge, Dustin

AU - Bale, Jim

AU - Barbouth, Deborah

AU - Batzli, Gabriel F.

AU - Bayrak-Toydemir, Pinar

AU - Beggs, Alan H.

AU - Bejerano, Gill

AU - Bellen, Hugo J.

AU - Bernstein, Jonathan A.

AU - Berry, Gerard T.

AU - Bican, Anna

AU - Bick, David P.

AU - Birch, Camille L.

AU - Bivona, Stephanie

AU - Bohnsack, John

AU - Lanpher, Brendan C.

AU - Lanza, Ian R.

AU - Morava-Kozicz, Eva

AU - Oglesbee, Devin

PY - 2019/9/5

Y1 - 2019/9/5

N2 - (The American Journal of Human Genetics 105, 413–424; August 1, 2019) In the originally published version of this article, Figures 3B and 3C included the allele name “sisy” but the correct term is “wrd37,” as appears in the rest of the article. In addition, there are two edits in Figure 3A: Thr125 has been highlighted instead of Thr124 and “Patient variants” has been changed to “Protein variants.” All these changes are reflected in the figure below and in the article online. The authors regret these errors. [Figure presented] [Figure presented]

AB - (The American Journal of Human Genetics 105, 413–424; August 1, 2019) In the originally published version of this article, Figures 3B and 3C included the allele name “sisy” but the correct term is “wrd37,” as appears in the rest of the article. In addition, there are two edits in Figure 3A: Thr125 has been highlighted instead of Thr124 and “Patient variants” has been changed to “Protein variants.” All these changes are reflected in the figure below and in the article online. The authors regret these errors. [Figure presented] [Figure presented]

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UR - http://www.scopus.com/inward/citedby.url?scp=85071704445&partnerID=8YFLogxK

U2 - 10.1016/j.ajhg.2019.07.017

DO - 10.1016/j.ajhg.2019.07.017

M3 - Comment/debate

C2 - 31491411

AN - SCOPUS:85071704445

VL - 105

SP - 672

EP - 674

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

SN - 0002-9297

IS - 3

ER -