×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients.
19453301
2009
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
Compound heterozygosity in the SPG4 gene causes hereditary spastic paraplegia.
18190593
2008
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
Compound heterozygosity in the SPG4 gene causes hereditary spastic paraplegia.
18190593
2008
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegia.
17100993
2006
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition.
17101632
2006
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegia.
17100993
2006
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition.
17101632
2006
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene.
15326248
2004
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene.
15326248
2004
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation.
14681884
2003
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation.
14681884
2003
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia.
11309678
2001
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia.
11309678
2001
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.
10699187
2000
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.
10699187
2000
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.
10610178
1999
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.
10610178
1999