rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies.
27292316
2016
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders.
12552055
2003
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females.
12390976
2002
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.
11175293
2001
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.
11601509
2001
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene.
11468322
2001
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence.
10807542
2000
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
Characterization of mutations in the gene doublecortin in patients with double cortex syndrome.
9989615
1999
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1.
10441340
1999
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia.
10369164
1999
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH).
9618162
1998
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects.
9668176
1998
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein.
9489700
1998
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.
9817918
1998
rs398124557
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
Lissencephaly, X-Linked, 1
0.700
GeneticVariation
UNIPROT
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome.
9489699
1998