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ARX mutations in X-linked lissencephaly with abnormal genitalia
- 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.
- Subjects :
- Heart Defects, Congenital
Male
Candidate gene
Microcephaly
DNA Mutational Analysis
Mutation, Missense
Lissencephaly
Biology
Genitalia, Male
medicine.disease_cause
Basal Ganglia
Structure-Activity Relationship
Fatal Outcome
Cell Movement
Cryptorchidism
medicine
Humans
Point Mutation
Abnormalities, Multiple
education
X chromosome
Sequence Deletion
Genetics
Cerebral Cortex
Homeodomain Proteins
Mutation
education.field_of_study
Hypospadias
Epilepsy
Point mutation
Infant, Newborn
medicine.disease
Pedigree
Protein Structure, Tertiary
Amino Acid Substitution
Aristaless related homeobox
Mental Retardation, X-Linked
Homeobox
Neurology (clinical)
Transcription Factors
Subjects
Details
- ISSN :
- 1526632X
- Volume :
- 61
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Neurology
- Accession number :
- edsair.doi.dedup.....6404e979e15343469f99d2154d72b748