Brain malformations and mutations inα- andβ-tubulin genes: a review of the literature and description of two new cases

Overlapping cortical malformations and mutations in TUBB2B and TUBA1A

(2013) Thomas D. Cushion et al.   BRAIN

A developmental and genetic classification for malformations of cortical development: update 2012

(2012) A. James Barkovich et al.   BRAIN

Lissencephaly with marked ventricular dilation, agenesis of corpus callosum, and cerebellar hypoplasia caused by TUBA1A mutation

(2012) Akihisa Okumura et al.   BRAIN & DEVELOPMENT

A novel mutation in the β-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance

(2012) ROMINA ROMANIELLO et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations

(2012) Renzo Guerrini et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria

(2012) Karine Poirier et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation

(2012) Gustav Y. Cederquist et al.   HUMAN MOLECULAR GENETICS

Lissencephaly and Band Heterotopia: LIS1, TUBA1A, and DCX Mutations in Hungary

(2012) Attila Mokánszki et al.   JOURNAL OF CHILD NEUROLOGY

TUBA1A Mutation-Associated Lissencephaly: Case Report and Review of the Literature

(2012) Aman P.S. Sohal et al.   PEDIATRIC NEUROLOGY

Phenotypic spectrum of the tubulin-related disorders and functional implications of disease-causing mutations

(2011) Max A Tischfield et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations

(2011) Roxana Kariminejad et al.   HUMAN MUTATION

TUBA1A mutations: From isolated lissencephaly to familial polymicrogyria

(2011) A. C. Jansen et al.   NEUROLOGY

MicroTUB(B3)ules and Brain Development

(2010) Karun K. Singh et al.   CELL

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

(2010) Max A. Tischfield et al.   CELL

Congenital Bilateral Perisylvian Syndrome in a Monozygotic Twin with Intra-uterine Death ot the Co-twin

(2010) Patrick Van Bogaert et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

The Role of Tuba1a in Adult Hippocampal Neurogenesis and the Formation of the Dentate Gyrus

(2010) David A. Keays et al.   DEVELOPMENTAL NEUROSCIENCE

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

Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway

(2010) Guoling Tian et al.   HUMAN MOLECULAR GENETICS

TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins

(2010) Ravinesh A. Kumar et al.   HUMAN MOLECULAR GENETICS

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

Refining the phenotype of α-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly

(2009) DJ Morris-Rosendahl et al.   CLINICAL GENETICS

The β-tubulin geneTUBB2Bis involved in a large spectrum of neuronal migration disorders

(2009) V Uribe   CLINICAL GENETICS

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

(2009) Xavier Hubert Jaglin et al.   NATURE GENETICS

Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defects

(2009) Xavier H. Jaglin et al.   TRENDS IN GENETICS

Midbrain-hindbrain involvement in lissencephalies

(2008) P. Jissendi-Tchofo et al.   NEUROLOGY