Concepedia

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

Susan E. Hong, Yin Yao Shugart, David T. Huang, Saad Al Shahwan, P. Ellen Grant, Jonathan O'B. Hourihane, Neil D. Martin, Christopher A. Walsh

Nature Genetics · 2000 · 878 citations · 25 references

DOI

Concepts

References

25

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

Marvin B. Shapiro, Periannan Senapathy · Nucleic Acids Research · 1987 · 2.3K citations · Full text

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A protein related to extracellular matrix proteins deleted in the mouse mutant reeler

Gabriella D’Arcangelo, Graham G. Miao, Shu‐Cheng Chen et al. · Nature · 1995 · 1.8K citations

, , +12

Reeler/Disabled-like Disruption of Neuronal Migration in Knockout Mice Lacking the VLDL Receptor and ApoE Receptor 2

Marion Trommsdorff, Michael Gotthardt, Thomas Hiesberger et al. · Cell · 1999 · 1.3K citations · Full text

, , +15

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

, , +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

, , +3