Case reports: novel TUBG1 mutations with milder neurodevelopmental presentations

Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1

(2018) Stefanie Brock et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Tubulin genes and malformations of cortical development

(2018) Romina Romaniello et al.   European Journal of Medical Genetics

Early identification of treatable inborn errors of metabolism in children with intellectual disability: The Treatable Intellectual Disability Endeavor protocol in British Columbia

(2017) Clara DM van Karnebeek et al.   Paediatrics & Child Health

Malformations of cortical development

(2016) Rahul S. Desikan et al.   ANNALS OF NEUROLOGY

The wide spectrum of tubulinopathies: what are the key features for the diagnosis?

(2014) Nadia Bahi-Buisson et al.   BRAIN

Molecular insight into γ–γ tubulin lateral interactions within the γ-tubulin ring complex (γ-TuRC)

(2014) Charu Suri et al.   JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN

GTP regulates the microtubule nucleation activity of γ-tubulin

(2013) Linda Gombos et al.   NATURE CELL BIOLOGY

Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly

(2013) Karine Poirier et al.   NATURE GENETICS

Congenital Microcephaly with a Simplified Gyral Pattern: Associated Findings and Their Significance

(2011) Y. Adachi et al.   AMERICAN JOURNAL OF NEURORADIOLOGY

The lattice as allosteric effector: Structural studies of   - and  -tubulin clarify the role of GTP in microtubule assembly

(2008) L. M. Rice et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA