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

doi:10.1016/j.ajhg.2019.07.017

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 journal › Comment/debate

7 Scopus citations

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.

Original language	English
Pages (from-to)	672-674
Number of pages	3
Journal	American journal of human genetics
Volume	105
Issue number	3
DOIs	https://doi.org/10.1016/j.ajhg.2019.07.017
State	Published - Sep 5 2019

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Undiagnosed Diseases Network (2019). 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)). American journal of human genetics, 105(3), 672-674. https://doi.org/10.1016/j.ajhg.2019.07.017

Undiagnosed Diseases Network. / 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)). In: American journal of human genetics. 2019 ; Vol. 105, No. 3. pp. 672-674.

@article{0533c60e9b49455493b38e9a91b87313,

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.",

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 Cole, {F. Sessions} and Stephen Pak and Timothy Schedl and Jimann Shin and Lilianna Solnica-Krezel and Jennifer Wambach",

note = "Publisher Copyright: {\textcopyright} 2019",

year = "2019",

month = sep,

day = "5",

doi = "10.1016/j.ajhg.2019.07.017",

language = "English",

volume = "105",

pages = "672--674",

journal = "American journal of human genetics",

issn = "0002-9297",

number = "3",

}

Undiagnosed Diseases Network 2019, '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))', American journal of human genetics, vol. 105, no. 3, pp. 672-674. https://doi.org/10.1016/j.ajhg.2019.07.017

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.
In: American journal of human genetics, Vol. 105, No. 3, 05.09.2019, p. 672-674.

Research output: Contribution to journal › Comment/debate

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 - Cole, F. Sessions

AU - Pak, Stephen

AU - Schedl, Timothy

AU - Shin, Jimann

AU - Solnica-Krezel, Lilianna

AU - Wambach, Jennifer

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.

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.

UR - http://www.scopus.com/inward/record.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

SN - 0002-9297

VL - 105

SP - 672

EP - 674

JO - American journal of human genetics

JF - American journal of human genetics

IS - 3

ER -

Undiagnosed Diseases Network. 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)). American journal of human genetics. 2019 Sep 5;105(3):672-674. doi: 10.1016/j.ajhg.2019.07.017

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))

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