|
rs137853016
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events.
|
27133561 |
2016 |
|
rs137853017
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events.
|
27133561 |
2016 |
|
rs137853018
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events.
|
27133561 |
2016 |
|
rs137853019
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events.
|
27133561 |
2016 |
|
rs137853016
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood.
|
24418350 |
2014 |
|
rs137853017
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood.
|
24418350 |
2014 |
|
rs137853018
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood.
|
24418350 |
2014 |
|
rs137853019
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood.
|
24418350 |
2014 |
|
rs140551762
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood.
|
24418350 |
2014 |
|
rs137853016
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in SACS cause atypical and late-onset forms of ARSACS.
|
20876471 |
2010 |
|
rs137853017
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in SACS cause atypical and late-onset forms of ARSACS.
|
20876471 |
2010 |
|
rs137853018
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in SACS cause atypical and late-onset forms of ARSACS.
|
20876471 |
2010 |
|
rs137853019
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in SACS cause atypical and late-onset forms of ARSACS.
|
20876471 |
2010 |
|
rs137853016
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel SACS gene mutation in a Tunisian family.
|
19529988 |
2009 |
|
rs137853017
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel SACS gene mutation in a Tunisian family.
|
19529988 |
2009 |
|
rs137853018
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel SACS gene mutation in a Tunisian family.
|
19529988 |
2009 |
|
rs137853019
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel SACS gene mutation in a Tunisian family.
|
19529988 |
2009 |
|
rs137853016
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia.
|
18465152 |
2008 |
|
rs137853016
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel genomic disorder: a deletion of the SACS gene leading to spastic ataxia of Charlevoix-Saguenay.
|
18398442 |
2008 |
|
rs137853016
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel SACS mutation in a Belgian family with sacsin-related ataxia.
|
17716690 |
2008 |
|
rs137853016
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): novel compound heterozygous mutations in the SACS gene.
|
18484239 |
2008 |
|
rs137853017
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia.
|
18465152 |
2008 |
|
rs137853017
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel SACS mutation in a Belgian family with sacsin-related ataxia.
|
17716690 |
2008 |
|
rs137853017
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): novel compound heterozygous mutations in the SACS gene.
|
18484239 |
2008 |
|
rs137853017
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel genomic disorder: a deletion of the SACS gene leading to spastic ataxia of Charlevoix-Saguenay.
|
18398442 |
2008 |