Original paper
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations
Abstract
Normal development of the cerebral cortex requires long-range migration of cortical neurons from proliferative regions deep in the brain. Lissencephaly (smooth null from lissos, meaning smooth, and encephalos, meaning brain) is a severe developmental disorder in which neuronal migration is impaired, leading to a thickened cerebral cortex whose normally folded contour is simplified and smooth. Two identified lissencephaly genes do not account for...
Paper Details
Title
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations
Published Date
Sep 1, 2000
Journal
Volume
26
Issue
1
Pages
93 - 96
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Notes
History