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))

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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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