rs104894106
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A novel missense mutation (L198R) in the Friedreich's ataxia gene.
|
10874325 |
2000 |
rs104894106
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
|
9989622 |
1999 |
rs104894106
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
The first cellular models based on frataxin missense mutations that reproduce spontaneously the defects associated with Friedreich ataxia.
|
19629184 |
2009 |
rs104894106
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.
|
9150176 |
1997 |
rs104894106
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.
|
10732799 |
1998 |
rs104894106
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Identification of a missense mutation in a Friedreich's ataxia patient: implications for diagnosis and carrier studies.
|
9779809 |
1998 |
rs104894105
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.
|
9150176 |
1997 |
rs104894105
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.
|
10732799 |
1998 |
rs104894105
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel missense mutation (L198R) in the Friedreich's ataxia gene.
|
10874325 |
2000 |
rs104894105
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
|
9989622 |
1999 |
rs104894105
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
The first cellular models based on frataxin missense mutations that reproduce spontaneously the defects associated with Friedreich ataxia.
|
19629184 |
2009 |
rs104894105
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Identification of a missense mutation in a Friedreich's ataxia patient: implications for diagnosis and carrier studies.
|
9779809 |
1998 |
rs104894107
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Identification of a missense mutation in a Friedreich's ataxia patient: implications for diagnosis and carrier studies.
|
9779809 |
1998 |
rs104894107
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.
|
10732799 |
1998 |
rs104894107
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
|
9989622 |
1999 |
rs104894107
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
The first cellular models based on frataxin missense mutations that reproduce spontaneously the defects associated with Friedreich ataxia.
|
19629184 |
2009 |
rs104894107
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel missense mutation (L198R) in the Friedreich's ataxia gene.
|
10874325 |
2000 |
rs104894107
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.
|
9150176 |
1997 |
rs138034837
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
|
|
|
rs138471431
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
|
|
|
rs139616452
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.
|
9150176 |
1997 |
rs139616452
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.
|
10732799 |
1998 |
rs139616452
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
|
9989622 |
1999 |
rs139616452
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
A novel missense mutation (L198R) in the Friedreich's ataxia gene.
|
10874325 |
2000 |
rs139616452
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Identification of a missense mutation in a Friedreich's ataxia patient: implications for diagnosis and carrier studies.
|
9779809 |
1998 |