Associated Papers
Pathogenic E2K mutation of doublecortin X (DCX) alters microtubule stabilisation and actin filament association.
Moslehi M et al.
Biochemical and Biophysical Research Communications, 2019
New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum.
Bahi-Buisson N et al.
Brain : a Journal of Neurology, 2013
Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyria.
Lawrence KM et al.
Epilepsia, 2010
The location of DCX mutations predicts malformation severity in X-linked lissencephaly.
Leger PL et al.
Neurogenetics, 2008
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