Erratum: De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders (The American Journal of Human Genetics (2019) 104(1) (139–156), (S0002929718304531) (10.1016/j.ajhg.2018.12.002))

Sara Reynhout; Sandra Jansen; Dorien Haesen; Siska van Belle; Sonja A. de Munnik; Ernie M. H. F. Bongers; Jolanda H. Schieving; Carlo Marcelis; Jeanne Amiel; Marlène Rio; Heather Mclaughlin; Roger Ladda; Susan Sell; Marjolein Kriek; Cacha M. P. C. D. Peeters-Scholte; Paulien A. Terhal; Koen L. van Gassen; Nienke Verbeek; Sonja Henry; Jessica Scott Schwoerer; Saleem Malik; Nicole Revencu; Carlos R. Ferreira; Ellen Macnamara; Hilde M. H. Braakman; Elise Brimble; Maura R. Z. Ruzhnikov; Matias Wagner; Philip Harrer; Dagmar Wieczorek; Alma Kuechler; Barak Tziperman; Ortal Barel; Bert B. A. de Vries; Christopher T. Gordon; Veerle Janssens; Lisenka E. L. M. Vissers

doi:10.1016/j.ajhg.2019.01.003

Erratum: De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders (The American Journal of Human Genetics (2019) 104(1) (139–156), (S0002929718304531) (10.1016/j.ajhg.2018.12.002))

Sara Reynhout, Sandra Jansen, Dorien Haesen, Siska van Belle, Sonja A. de Munnik, Ernie M. H. F. Bongers, Jolanda H. Schieving, Carlo Marcelis, Jeanne Amiel, Marlène Rio, Heather Mclaughlin, Roger Ladda, Susan Sell, Marjolein Kriek, Cacha M. P. C. D. Peeters-Scholte, Paulien A. Terhal, Koen L. van Gassen, Nienke Verbeek, Sonja Henry, Jessica Scott SchwoererSaleem Malik, Nicole Revencu, Carlos R. Ferreira, Ellen Macnamara, Hilde M. H. Braakman, Elise Brimble, Maura R. Z. Ruzhnikov, Matias Wagner, Philip Harrer, Dagmar Wieczorek, Alma Kuechler, Barak Tziperman, Ortal Barel, Bert B. A. de Vries, Christopher T. Gordon, Veerle Janssens, Lisenka E. L. M. Vissers

Clinical genetics

Research output: Contribution to journal › Erratum › Academic › peer-review

Abstract

(The American Journal of Human Genetics 104, 139–156; January 3, 2019) In the original version of this article published on December 27, 2018, Maura R.Z. Ruzhnikov's surname was unfortunately misspelled. It appears correctly here and online. The authors apologize for the error.

Original language	English
Pages (from-to)	357
Journal	American journal of human genetics
Volume	104
Issue number	2
DOIs	https://doi.org/10.1016/j.ajhg.2019.01.003
Publication status	Published - 7 Feb 2019

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10.1016/j.ajhg.2019.01.003

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Reynhout, S., Jansen, S., Haesen, D., van Belle, S., de Munnik, S. A., Bongers, E. M. H. F., ... Vissers, L. E. L. M. (2019). Erratum: De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders (The American Journal of Human Genetics (2019) 104(1) (139–156), (S0002929718304531) (10.1016/j.ajhg.2018.12.002)). American journal of human genetics, 104(2), 357. https://doi.org/10.1016/j.ajhg.2019.01.003

Reynhout, Sara ; Jansen, Sandra ; Haesen, Dorien ; van Belle, Siska ; de Munnik, Sonja A. ; Bongers, Ernie M. H. F. ; Schieving, Jolanda H. ; Marcelis, Carlo ; Amiel, Jeanne ; Rio, Marlène ; Mclaughlin, Heather ; Ladda, Roger ; Sell, Susan ; Kriek, Marjolein ; Peeters-Scholte, Cacha M. P. C. D. ; Terhal, Paulien A. ; van Gassen, Koen L. ; Verbeek, Nienke ; Henry, Sonja ; Schwoerer, Jessica Scott ; Malik, Saleem ; Revencu, Nicole ; Ferreira, Carlos R. ; Macnamara, Ellen ; Braakman, Hilde M. H. ; Brimble, Elise ; Ruzhnikov, Maura R. Z. ; Wagner, Matias ; Harrer, Philip ; Wieczorek, Dagmar ; Kuechler, Alma ; Tziperman, Barak ; Barel, Ortal ; de Vries, Bert B. A. ; Gordon, Christopher T. ; Janssens, Veerle ; Vissers, Lisenka E. L. M. / Erratum: De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders (The American Journal of Human Genetics (2019) 104(1) (139–156), (S0002929718304531) (10.1016/j.ajhg.2018.12.002)). In: American journal of human genetics. 2019 ; Vol. 104, No. 2. pp. 357.

@article{3e5e41f54f104716935f83bcc88c631b,

title = "Erratum: De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders (The American Journal of Human Genetics (2019) 104(1) (139–156), (S0002929718304531) (10.1016/j.ajhg.2018.12.002))",

abstract = "(The American Journal of Human Genetics 104, 139–156; January 3, 2019) In the original version of this article published on December 27, 2018, Maura R.Z. Ruzhnikov's surname was unfortunately misspelled. It appears correctly here and online. The authors apologize for the error.",

author = "Sara Reynhout and Sandra Jansen and Dorien Haesen and {van Belle}, Siska and {de Munnik}, {Sonja A.} and Bongers, {Ernie M. H. F.} and Schieving, {Jolanda H.} and Carlo Marcelis and Jeanne Amiel and Marl{\`e}ne Rio and Heather Mclaughlin and Roger Ladda and Susan Sell and Marjolein Kriek and Peeters-Scholte, {Cacha M. P. C. D.} and Terhal, {Paulien A.} and {van Gassen}, {Koen L.} and Nienke Verbeek and Sonja Henry and Schwoerer, {Jessica Scott} and Saleem Malik and Nicole Revencu and Ferreira, {Carlos R.} and Ellen Macnamara and Braakman, {Hilde M. H.} and Elise Brimble and Ruzhnikov, {Maura R. Z.} and Matias Wagner and Philip Harrer and Dagmar Wieczorek and Alma Kuechler and Barak Tziperman and Ortal Barel and {de Vries}, {Bert B. A.} and Gordon, {Christopher T.} and Veerle Janssens and Vissers, {Lisenka E. L. M.}",

year = "2019",

month = "2",

day = "7",

doi = "10.1016/j.ajhg.2019.01.003",

language = "English",

volume = "104",

pages = "357",

journal = "American journal of human genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "2",

}

Reynhout, S, Jansen, S, Haesen, D, van Belle, S, de Munnik, SA, Bongers, EMHF, Schieving, JH, Marcelis, C, Amiel, J, Rio, M, Mclaughlin, H, Ladda, R, Sell, S, Kriek, M, Peeters-Scholte, CMPCD, Terhal, PA, van Gassen, KL, Verbeek, N, Henry, S, Schwoerer, JS, Malik, S, Revencu, N, Ferreira, CR, Macnamara, E, Braakman, HMH, Brimble, E, Ruzhnikov, MRZ, Wagner, M, Harrer, P, Wieczorek, D, Kuechler, A, Tziperman, B, Barel, O, de Vries, BBA, Gordon, CT, Janssens, V & Vissers, LELM 2019, 'Erratum: De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders (The American Journal of Human Genetics (2019) 104(1) (139–156), (S0002929718304531) (10.1016/j.ajhg.2018.12.002))', American journal of human genetics, vol. 104, no. 2, pp. 357. https://doi.org/10.1016/j.ajhg.2019.01.003

Erratum: De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders (The American Journal of Human Genetics (2019) 104(1) (139–156), (S0002929718304531) (10.1016/j.ajhg.2018.12.002)). / Reynhout, Sara; Jansen, Sandra; Haesen, Dorien; van Belle, Siska; de Munnik, Sonja A.; Bongers, Ernie M. H. F.; Schieving, Jolanda H.; Marcelis, Carlo; Amiel, Jeanne; Rio, Marlène; Mclaughlin, Heather; Ladda, Roger; Sell, Susan; Kriek, Marjolein; Peeters-Scholte, Cacha M. P. C. D.; Terhal, Paulien A.; van Gassen, Koen L.; Verbeek, Nienke; Henry, Sonja; Schwoerer, Jessica Scott; Malik, Saleem; Revencu, Nicole; Ferreira, Carlos R.; Macnamara, Ellen; Braakman, Hilde M. H.; Brimble, Elise; Ruzhnikov, Maura R. Z.; Wagner, Matias; Harrer, Philip; Wieczorek, Dagmar; Kuechler, Alma; Tziperman, Barak; Barel, Ortal; de Vries, Bert B. A.; Gordon, Christopher T.; Janssens, Veerle; Vissers, Lisenka E. L. M.

In: American journal of human genetics, Vol. 104, No. 2, 07.02.2019, p. 357.

Research output: Contribution to journal › Erratum › Academic › peer-review

TY - JOUR

T1 - Erratum: De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders (The American Journal of Human Genetics (2019) 104(1) (139–156), (S0002929718304531) (10.1016/j.ajhg.2018.12.002))

AU - Reynhout, Sara

AU - Jansen, Sandra

AU - Haesen, Dorien

AU - van Belle, Siska

AU - de Munnik, Sonja A.

AU - Bongers, Ernie M. H. F.

AU - Schieving, Jolanda H.

AU - Marcelis, Carlo

AU - Amiel, Jeanne

AU - Rio, Marlène

AU - Mclaughlin, Heather

AU - Ladda, Roger

AU - Sell, Susan

AU - Kriek, Marjolein

AU - Peeters-Scholte, Cacha M. P. C. D.

AU - Terhal, Paulien A.

AU - van Gassen, Koen L.

AU - Verbeek, Nienke

AU - Henry, Sonja

AU - Schwoerer, Jessica Scott

AU - Malik, Saleem

AU - Revencu, Nicole

AU - Ferreira, Carlos R.

AU - Macnamara, Ellen

AU - Braakman, Hilde M. H.

AU - Brimble, Elise

AU - Ruzhnikov, Maura R. Z.

AU - Wagner, Matias

AU - Harrer, Philip

AU - Wieczorek, Dagmar

AU - Kuechler, Alma

AU - Tziperman, Barak

AU - Barel, Ortal

AU - de Vries, Bert B. A.

AU - Gordon, Christopher T.

AU - Janssens, Veerle

AU - Vissers, Lisenka E. L. M.

PY - 2019/2/7

Y1 - 2019/2/7

N2 - (The American Journal of Human Genetics 104, 139–156; January 3, 2019) In the original version of this article published on December 27, 2018, Maura R.Z. Ruzhnikov's surname was unfortunately misspelled. It appears correctly here and online. The authors apologize for the error.

AB - (The American Journal of Human Genetics 104, 139–156; January 3, 2019) In the original version of this article published on December 27, 2018, Maura R.Z. Ruzhnikov's surname was unfortunately misspelled. It appears correctly here and online. The authors apologize for the error.

UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85059846107&origin=inward

UR - https://www.ncbi.nlm.nih.gov/pubmed/30735662

U2 - 10.1016/j.ajhg.2019.01.003

DO - 10.1016/j.ajhg.2019.01.003

M3 - Erratum

C2 - 30735662

VL - 104

SP - 357

JO - American journal of human genetics

JF - American journal of human genetics

SN - 0002-9297

IS - 2

ER -

Reynhout S, Jansen S, Haesen D, van Belle S, de Munnik SA, Bongers EMHF et al. Erratum: De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders (The American Journal of Human Genetics (2019) 104(1) (139–156), (S0002929718304531) (10.1016/j.ajhg.2018.12.002)). American journal of human genetics. 2019 Feb 7;104(2):357. https://doi.org/10.1016/j.ajhg.2019.01.003