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

Author:

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,Scott Schwoerer Jessica,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.

Funder

IAP program of the Belgian federal government

Research Foundation-Flanders

University of Leuven

Flemish Agency for Innovation by Science and Technology

Netherlands Organization for Health Research and Development

Wellcome Trust

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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