The diagnostic challenges of congenital mirror movements and hand stereotypies in a case with TUBB3-associated tubulinopathy

[1]  D. Lev,et al.  Congenital Mirror Movements Associated With Brain Malformations , 2021, Journal of child neurology.

[2]  D. Lev,et al.  Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features. , 2020, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

[3]  X. Wei,et al.  TUBA1A Mutation Associated With Eye Abnormalities in Addition to Brain Malformation. , 2015, Pediatric neurology.

[4]  C. Galléa,et al.  One hand clapping: lateralization of motor control , 2015, Front. Neuroanat..

[5]  N. Boddaert,et al.  The wide spectrum of tubulinopathies: what are the key features for the diagnosis? , 2014, Brain : a journal of neurology.

[6]  C. Fallet-Bianco,et al.  Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects. , 2010, Human molecular genetics.

[7]  C. Bonnet,et al.  Developmental and benign movement disorders in childhood , 2010, Movement disorders : official journal of the Movement Disorder Society.

[8]  T. Meitinger,et al.  Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance , 2010, Cell.