New insights into genotype–phenotype correlations for the doublecortin-related lissencephaly spectrum

Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance

(2010) Max A. Tischfield et al.   CELL

Spontaneous Epileptic Manifestations in a DCX Knockdown Model of Human Double Cortex

(2010) Damien Lapray et al.   CEREBRAL CORTEX

Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009

(2010) Anne T. Berg et al.   EPILEPSIA

Mutations in the neuronal β-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects

(2010) Karine Poirier et al.   HUMAN MOLECULAR GENETICS

Template-free 13-protofilament microtubule–MAP assembly visualized at 8 Å resolution

(2010) Franck J. Fourniol et al.   JOURNAL OF CELL BIOLOGY

Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia

(2009) Mohammad R. Abdollahi et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Abnormal Network Activity in a Targeted Genetic Model of Human Double Cortex

(2009) J. B. Ackman et al.   JOURNAL OF NEUROSCIENCE

Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria

(2009) Xavier Hubert Jaglin et al.   NATURE GENETICS

Different structures involved during ictal and interictal epileptic activity in malformations of cortical development: an EEG-fMRI study

(2008) L. Tyvaert et al.   BRAIN

Characterization of the HeCo Mutant Mouse: A New Model of Subcortical Band Heterotopia Associated with Seizures and Behavioral Deficits

(2008) Alexandre Croquelois et al.   CEREBRAL CORTEX

Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia

(2008) Eden V Haverfield et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia

(2008) Russell J. Ferland et al.   HUMAN MOLECULAR GENETICS

The location of DCX mutations predicts malformation severity in X-linked lissencephaly

(2008) Pierre-Louis Leger et al.   NEUROGENETICS