transporter (ABCA4) gene have been associated with several forms of macular degenerations. Because the high complexity of the molecular genotype makes scan-ning of the ABCA4 gene cumbersome, we describe here the first use of denaturing HPLC (DHPLC) to screen for ABCA4 mutations. Methods: Temperature conditions were designed for all 50 exons based on effective separation of 83 samples carrying 86 sequence variations and 19 mutagenized controls. For validation, samples from 23 previously characterized Stargardt patients were subjected to DH-PLC profiling. Subsequently, samples from a cohort of 30 patients affected by various forms of macular degen-eration were subjected to DHPLC scanning under the same conditions. Results: DHPLC profiling not...
Purpose: To resolve the spectrum of causative retina-specific ATP-binding cassette transporter gene ...
Journal ArticlePURPOSE: A 5-bp deletion in ELOVL4, a photoreceptor-specific gene, has been associate...
Here we report novel mutations in ABCA4 with the underlying phenotype in a large French cohort with ...
transporter (ABCA4) gene have been associated with several forms of macular degenerations. Because t...
Mutations in the ABCA1 gene are the cause of familial high density lipoprotein deficiency (FHD). Bec...
: The ABCA4 gene is the most frequently mutated Mendelian retinopathy-associated gene. Biallelic var...
Stargardt disease (STGD) is a common autosomal recessive maculopathy of early and young-adult onset ...
Genetic variation in the ABCR (ABCA4) gene has been associated with five distinct retinal phenotypes...
Stargardt disease (STGD) is a common autosomal recessive maculopathy of early and young-adult onset ...
Genetic variation in the ABCR (ABCA4) gene has been associated with five distinct retinal phenotypes...
Macular dystrophies are a group of individually rare but collectively common inherited retinal dystr...
AbstractBackgroundThe commonest genetic form of juvenile or early adult onset macular degeneration i...
Macular degenerations (MDs) are a subgroup of retinal disorders characterized by central vision loss...
Abstract Background The commonest genetic form of juvenile or early adult onset macular degeneration...
Purpose. Age-related macular degeneration (AMD) is a heterogeneous condition of high prevalence and ...
Purpose: To resolve the spectrum of causative retina-specific ATP-binding cassette transporter gene ...
Journal ArticlePURPOSE: A 5-bp deletion in ELOVL4, a photoreceptor-specific gene, has been associate...
Here we report novel mutations in ABCA4 with the underlying phenotype in a large French cohort with ...
transporter (ABCA4) gene have been associated with several forms of macular degenerations. Because t...
Mutations in the ABCA1 gene are the cause of familial high density lipoprotein deficiency (FHD). Bec...
: The ABCA4 gene is the most frequently mutated Mendelian retinopathy-associated gene. Biallelic var...
Stargardt disease (STGD) is a common autosomal recessive maculopathy of early and young-adult onset ...
Genetic variation in the ABCR (ABCA4) gene has been associated with five distinct retinal phenotypes...
Stargardt disease (STGD) is a common autosomal recessive maculopathy of early and young-adult onset ...
Genetic variation in the ABCR (ABCA4) gene has been associated with five distinct retinal phenotypes...
Macular dystrophies are a group of individually rare but collectively common inherited retinal dystr...
AbstractBackgroundThe commonest genetic form of juvenile or early adult onset macular degeneration i...
Macular degenerations (MDs) are a subgroup of retinal disorders characterized by central vision loss...
Abstract Background The commonest genetic form of juvenile or early adult onset macular degeneration...
Purpose. Age-related macular degeneration (AMD) is a heterogeneous condition of high prevalence and ...
Purpose: To resolve the spectrum of causative retina-specific ATP-binding cassette transporter gene ...
Journal ArticlePURPOSE: A 5-bp deletion in ELOVL4, a photoreceptor-specific gene, has been associate...
Here we report novel mutations in ABCA4 with the underlying phenotype in a large French cohort with ...