rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease.
|
9973280 |
1999 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Frequency of ABCA4 mutations in 278 Spanish controls: an insight into the prevalence of autosomal recessive Stargardt disease.
|
18977788 |
2009 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Late-onset Stargardt disease is associated with missense mutations that map outside known functional regions of ABCR (ABCA4).
|
11379881 |
2001 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
A |
0.820 |
GeneticVariation
|
CLINVAR |
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.
|
9054934 |
1997 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies.
|
9781034 |
1998 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
BEFREE |
To report genetic and phenotypic discordance across two generations of a family with autosomal recessive Stargardt disease (STGD1) and to compare pathogenicities of the G1961E and A1038V alleles of the ATP-binding cassette transporter, subfamily A, member 4 (ABCA4) gene.
|
22312191 |
2012 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Whole exome sequencing detects homozygosity for ABCA4 p.Arg602Trp missense mutation in a pediatric patient with rapidly progressive retinal dystrophy.
|
24444108 |
2014 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration.
|
10958763 |
2000 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1).
|
11594993 |
2001 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Differential phospholipid substrates and directional transport by ATP-binding cassette proteins ABCA1, ABCA7, and ABCA4 and disease-causing mutants.
|
24097981 |
2013 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Spectrum of ABCA4 (ABCR) gene mutations in Spanish patients with autosomal recessive macular dystrophies.
|
11385708 |
2001 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease.
|
10711710 |
2000 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease.
|
10612508 |
1999 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degeneration.
|
11527935 |
2001 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR gene.
|
10206579 |
1999 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
BEFREE |
In order to further understand the contribution of this gene to the susceptibility to STGD and RP, we analyzed three unrelated STGD families and one autosomal recessive RP family specifically for the more common variants (A1038V, G1961E, 2588G-->C, R943Q or 2828G-->A) in the ABCA4 gene.
|
18506364 |
2008 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
An analysis of allelic variation in the ABCA4 gene.
|
11328725 |
2001 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Mapping of the rod photoreceptor ABC transporter (ABCR) to 1p21-p22.1 and identification of novel mutations in Stargardt's disease.
|
9490294 |
1998 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.
|
9054934 |
1997 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Complex inheritance of ABCR mutations in Stargardt disease: linkage disequilibrium, complex alleles, and pseudodominance.
|
10746567 |
2000 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
Complete exon-intron structure of the retina-specific ATP binding transporter gene (ABCR) allows the identification of novel mutations underlying Stargardt disease.
|
9503029 |
1998 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease.
|
10090887 |
1999 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
|
0.820 |
GeneticVariation
|
UNIPROT |
An analysis of ABCR mutations in British patients with recessive retinal dystrophies.
|
10634594 |
2000 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
A |
0.820 |
CausalMutation
|
CLINVAR |
Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results.
|
25087612 |
2014 |
rs61751374
|
|
STARGARDT DISEASE 1 (disorder)
|
A |
0.820 |
CausalMutation
|
CLINVAR |
Stargardt disease caused by a rare combination of double homozygous mutations.
|
24509150 |
2013 |