PAK3 mutations responsible for severe intellectual disability and callosal agenesis inhibit cell migration

Duarte, K; Heide, S; Poea-Guyon, S; Rousseau, V; Depienne, C; Rastetter, A; Nava, C; Attie-Bitach, T; Razavi, F; Martinovic, J; Moutard, ML; Cherfils, J; Mignot, C; Heron, D; Barnier, JV

Barnier, JV (corresponding author), Paris Sud Univ, Paris Saclay Inst Neurosci Neuro PSI CNRS, Dept Cognit & Behav, UMR 9197, F-91400 Orsay, France.; Barnier, JV (corresponding author), Paris Saclay Univ, Paris Saclay Inst Neurosci Neuro PSI CNRS, Dept Cognit & Behav, UMR 9197, F-91400 Orsay, France.; Heron, D (corresponding author), GH Pitie Salpetriere, AP HP, Dept Genet, Reference Ctr Intellectual Disabil Rare Causes, F-75013 Paris, France.

NEUROBIOLOGY OF DISEASE, 2020; 136 ():

Abstract

Corpus callosum agenesis (CCA) is a brain malformation associated with a wide clinical spectrum including intellectual disability (ID) and an etiopath......

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