Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans

Author:

Keays David A.,Tian Guoling,Poirier Karine,Huang Guo-Jen,Siebold Christian,Cleak James,Oliver Peter L.,Fray Martin,Harvey Robert J.,Molnár Zoltán,Piñon Maria C.,Dear Neil,Valdar William,Brown Steve D.M.,Davies Kay E.,Rawlins J. Nicholas P.,Cowan Nicholas J.,Nolan Patrick,Chelly Jamel,Flint Jonathan

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference46 articles.

1. Time of neuron origin in the hippocampal region. An autoradiographic study in the mouse;Angevine;Exp. Neurol.,1965

2. A comparison of GluR-A-deficient and wild-type mice on a test battery assessing sensorimotor, affective, and cognitive behaviors;Bannerman;Behav. Neurosci.,2004

3. Functional overlap between retinitis pigmentosa 2 protein and the tubulin-specific chaperone cofactor C;Bartolini;J. Biol. Chem.,2002

4. QTLCartographer: a suite of programs for mapping quantitative trait loci. Abstracts to Plant Genome, IV;Basten,1996

5. Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification;Boycott;Am. J. Hum. Genet.,2005

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