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))
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Publication date
2019-02-07
Authors
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
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Supervisors
Document Type
Comment
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taverne
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.
Keywords
Taverne, Genetics, Genetics(clinical)
Citation
Reynhout, S, Jansen, S, Haesen, D, van Belle, S, de Munnik, S A, Bongers, E M H F, Schieving, J H, Marcelis, C, Amiel, J, Rio, M, Mclaughlin, H, Ladda, R, Sell, S, Kriek, M, Peeters-Scholte, C M P C D, Terhal, P A, van Gassen, K L, Verbeek, N, Henry, S, Schwoerer, J S, Malik, S, Revencu, N, Ferreira, C R, Macnamara, E, Braakman, H M H, Brimble, E, Ruzhnikov, M R Z, Wagner, M, Harrer, P, Wieczorek, D, Kuechler, A, Tziperman, B, Barel, O, de Vries, B B A, Gordon, C T, Janssens, V & 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, vol. 104, no. 2, pp. 357-357. https://doi.org/10.1016/j.ajhg.2019.01.003