| Literature DB >> 12874405 |
G Uyanik1, L Aigner, P Martin, C Gross, D Neumann, H Marschner-Schäfer, U Hehr, J Winkler.
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.Entities:
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Year: 2003 PMID: 12874405 DOI: 10.1212/01.wnl.0000079371.19562.ba
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910