A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation ofKIF2A

Microtubule Destabilizer KIF2A Undergoes Distinct Site-Specific Phosphorylation Cascades that Differentially Affect Neuronal Morphogenesis

(2015) Tadayuki Ogawa et al.   Cell Reports

The genetics of lissencephaly

(2014) Andrew E. Fry et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Congenital Brain Abnormalities: An Update on Malformations of Cortical Development and Infratentorial Malformations

(2014) Eugen Boltshauser et al.   SEMINARS IN NEUROLOGY

Aurora B and Kif2A control microtubule length for assembly of a functional central spindle during anaphase

(2013) Ryota Uehara et al.   JOURNAL OF CELL BIOLOGY

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

(2013) Karine Poirier et al.   NATURE GENETICS

Cytoskeleton in action: lissencephaly, a neuronal migration disorder

(2012) Hyang Mi Moon et al.   Wiley Interdisciplinary Reviews-Developmental Biology

Molecular Genetics of Neuronal Migration Disorders

(2011) Judy S. Liu   Current Neurology and Neuroscience Reports

Dystroglycanopathies: coming into focus

(2011) Caroline Godfrey et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Persistent hyperplastic primary vitreous: congenital malformation of the eye

(2009) Barkur S Shastry   CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY