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1
De novo mutations affecting the catalytic Cα subunit of PP2..:
Reynhout, S
;
Jansen, S
;
Haesen, D
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2018.12.002. , 2019
Link:
https://push-zb.helmholtz-muenchen.de/frontdoor.php?so..
RT Journal T1
De novo mutations affecting the catalytic Cα subunit of PP2A (PPP2CA) cause syndromic intellectual disability resembling other PP2A-related neurodevelopmental disorders
UL https://suche.suub.uni-bremen.de/peid=base-fthzmuenchen:oai:opus-zb.helmholtz-muenchen.de:55074&Exemplar=1&LAN=DE A1 Reynhout, S A1 Jansen, S A1 Haesen, D A1 van Belle, S A1 de Munnik, S.A A1 Bongers, E.M.H.F A1 Schieving, J.H A1 Marcelis, C.L A1 Amiel, J A1 Rio, M A1 Mclaughlin, H A1 Ladda, R A1 Sell, S A1 Kriek, M A1 Peeters-Scholte, C.M.P.C.D A1 Terhal, P.A A1 van Gassen, K.L A1 Verbeek, N A1 Henry, S A1 Scott Schwoerer, J A1 Malik, S A1 Revencu, N A1 Ferreira, C.R A1 Macnamara, E A1 Braakman, H.M.H A1 Brimble, E A1 Ruznikov, M.R.Z A1 Wagner, M A1 Harrer, P- A1 Wieczorek, D A1 Kuechler, A A1 Tziperman, B A1 Barel, O A1 de Vries, B.B.A A1 Gordon, C.T A1 Janssens, V A1 Vissers, L.E.L.M PB Cell Press YR 2019 K1 De Novo Mutation K1 Epilepsy K1 Intellectual Disability K1 Pp2a K1 Pp2a-related Neurodevelopmental Disorders K1 Ppp2ca K1 Syndrome JF info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2018.12.002 LK http://dx.doi.org/https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=55074 DO https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=55074 SF ELIB - SuUB Bremen
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