SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
Biomarker
|
disease |
CTD_human |
|
|
|
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease.
|
9635427 |
1998 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
GeneticVariation
|
disease |
UNIPROT |
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease.
|
9635427 |
1998 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
CausalMutation
|
disease |
CLINVAR |
Paraplegin gene analysis in hereditary spastic paraparesis (HSP) pedigrees in northeast England.
|
11222789 |
2001 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
Biomarker
|
disease |
MGD |
Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport.
|
14722615 |
2004 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
CausalMutation
|
disease |
CLINVAR |
A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia.
|
14985266 |
2004 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
GeneticVariation
|
disease |
UNIPROT |
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia.
|
16534102 |
2006 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
CausalMutation
|
disease |
CLINVAR |
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia.
|
16534102 |
2006 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
GermlineCausalMutation
|
disease |
ORPHANET |
A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation.
|
17646629 |
2007 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
GeneticVariation
|
disease |
UNIPROT |
A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation.
|
17646629 |
2007 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
CausalMutation
|
disease |
CLINVAR |
A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia.
|
18200586 |
2008 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
GeneticVariation
|
disease |
BEFREE |
Spastic paraplegia type 7 (SPG7) is an autosomal recessive form of hereditary spastic paraparesis (ARHSP) caused by mutations in paraplegin, a subunit of an ATP-dependent AAA-protease located within the inner mitochondrial membrane.
|
18563470 |
2008 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
CausalMutation
|
disease |
CLINVAR |
Hereditary spastic paraplegia caused by the novel mutation 1047insC in the SPG7 gene.
|
18563470 |
2008 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
CausalMutation
|
disease |
CLINVAR |
Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes.
|
18799786 |
2008 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
GeneticVariation
|
disease |
CLINVAR |
Functional evaluation of paraplegin mutations by a yeast complementation assay.
|
20186691 |
2010 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
CausalMutation
|
disease |
CLINVAR |
Functional evaluation of paraplegin mutations by a yeast complementation assay.
|
20186691 |
2010 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
GeneticVariation
|
disease |
UNIPROT |
Functional evaluation of paraplegin mutations by a yeast complementation assay.
|
20186691 |
2010 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
CausalMutation
|
disease |
CLINVAR |
Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients.
|
21623769 |
2011 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
GeneticVariation
|
disease |
CLINVAR |
Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients.
|
21623769 |
2011 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
GeneticVariation
|
disease |
BEFREE |
AFG3L2 forms either a homo-oligomeric isoenzyme or a hetero-oligomeric complex with paraplegin, a homologous protein mutated in hereditary spastic paraplegia type 7 (SPG7).
|
22022284 |
2011 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V.
|
22571692 |
2013 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
GeneticVariation
|
disease |
CLINVAR |
SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V.
|
22571692 |
2013 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V.
|
22571692 |
2013 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
CausalMutation
|
disease |
CLINVAR |
SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V.
|
22571692 |
2013 |
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
|
0.930 |
CausalMutation
|
disease |
CLINVAR |
Genotype-phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort.
|
22964162 |
2012 |