Genomic Structure, Chromosomal Mapping, and Expression Pattern of HumanDCAMKL1(KIAA0369), a Homologue ofDCX(XLIS)

doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein

Joseph G. Gleeson, Kristina M. Allen, Jeremy W. Fox et al. · Cell · 1998 · 1.1K citations · Full text

Medicine, Genetics, Molecular Genetics +13

Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit-like repeats

Orly Reiner, Romeo Carrozzo, Ying H. Shen et al. · Nature · 1993 · 1.1K citations

Life Sciences, Genetics, Molecular Genetics +3

Prediction of the Coding Sequences of Unidentified Human Genes. IX. The Complete Sequences of 100 New cDNA Clones from Brain Which Can Code for Large Proteins in vitro

DNA Research · 1998 · 846 citations · Full text

Life Sciences, Genetics, Molecular Biology +16

A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome

Vincent des Portes, Jean Marc Pinard, Pierre Billuart et al. · Cell · 1998 · 738 citations · Full text

Life Sciences, Genetics, Neuroscience +17

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation

Daniela T. Pilz · Human Molecular Genetics · 1998 · 355 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17