rs121917745
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population.
|
12960219 |
2003 |
rs121917745
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophy.
|
23878505 |
2013 |
rs121917745
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.
|
11095629 |
2000 |
rs121917745
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.
|
9501220 |
1998 |
rs121917745
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa, using microsatellite markers.
|
15557452 |
2004 |
rs121917745
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Next-generation genetic testing for retinitis pigmentosa.
|
22334370 |
2012 |
rs61752871
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Next-generation genetic testing for retinitis pigmentosa.
|
22334370 |
2012 |
rs61752871
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.
|
9501220 |
1998 |
rs61752871
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population.
|
12960219 |
2003 |
rs61752871
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa, using microsatellite markers.
|
15557452 |
2004 |
rs61752871
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophy.
|
23878505 |
2013 |
rs61752871
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.
|
11095629 |
2000 |
rs61752909
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.
|
9501220 |
1998 |
rs61752909
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa, using microsatellite markers.
|
15557452 |
2004 |
rs61752909
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population.
|
12960219 |
2003 |
rs61752909
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.
|
11095629 |
2000 |
rs61752909
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Next-generation genetic testing for retinitis pigmentosa.
|
22334370 |
2012 |
rs61752909
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophy.
|
23878505 |
2013 |
rs62637004
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Next-generation genetic testing for retinitis pigmentosa.
|
22334370 |
2012 |
rs62637004
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.
|
9501220 |
1998 |
rs62637004
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.
|
11095629 |
2000 |
rs62637004
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa, using microsatellite markers.
|
15557452 |
2004 |
rs62637004
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophy.
|
23878505 |
2013 |
rs62637004
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population.
|
12960219 |
2003 |
rs62642584
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population.
|
12960219 |
2003 |