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ARX mutations in X-linked lissencephaly with abnormal genitalia

Authors :
Juergen Winkler
Ute Hehr
D. Neumann
G. Uyanik
H. Marschner-Schafer
P. Martin
Ludwig Aigner
C. Gross
Source :
Neurology. 61(2)
Publication Year :
2003

Abstract

X-linked lissencephaly with abnormal genitalia (XLAG) is a distinct form of lissencephaly associated with absent corpus callosum. Recently, forms of syndromic and nonspecific X-linked mental retardation have been found to be associated with mutations in the Aristaless-related homeobox gene ARX. The authors assessed ARX as a candidate gene for XLAG in a genetic analysis of neuronal migration disorders and found two different point mutations in two XLAG pedigrees affecting the homeodomain of the protein, confirming that ARX is a causative gene for XLAG.

Details

ISSN :
1526632X
Volume :
61
Issue :
2
Database :
OpenAIRE
Journal :
Neurology
Accession number :
edsair.doi.dedup.....6404e979e15343469f99d2154d72b748