Interaction between LIS1 and doublecortin, two lissencephaly gene products
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/9/15/2205/9818866/092205.pdf
Reference26 articles.
1. A Classification Scheme for Malformations of Cortical Development
2. Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit-like repeats
3. A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome
4. doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein
5. LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation
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