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. 2019 Feb 7;104(2):357. doi: 10.1016/j.ajhg.2019.01.003

De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders

Sara Reynhout, Sandra Jansen, Dorien Haesen, Siska van Belle, Sonja A de Munnik, Ernie MHF Bongers, Jolanda H Schieving, Carlo Marcelis, Jeanne Amiel, Marlène Rio, Heather Mclaughlin, Roger Ladda, Susan Sell, Marjolein Kriek, Cacha MPCD 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 MH Braakman, Elise Brimble, Maura RZ Ruzhnikov, Matias Wagner, Philip Harrer, Dagmar Wieczorek, Alma Kuechler, Barak Tziperman, Ortal Barel, Bert BA de Vries, Christopher T Gordon, Veerle Janssens ∗, Lisenka ELM Vissers ∗∗
PMCID: PMC6369538  PMID: 30735662

(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.

Contributor Information

Veerle Janssens, Email: veerle.janssens@kuleuven.be.

Lisenka E.L.M. Vissers, Email: lisenka.vissers@radboudumc.nl.

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

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