MeSH term
Frequency | Condition_Probility | Humans | 45 | 0.0 |
United States | 2 | 0.0 |
ATP-Binding Cassette Transporters/*genetics | 26 | 11.0 |
Exons | 5 | 0.0 |
Introns | 3 | 0.0 |
Polymerase Chain Reaction | 6 | 0.0 |
*Polymorphism, Genetic | 2 | 0.0 |
Sequence Analysis, DNA | 8 | 0.0 |
*Variation (Genetics) | 5 | 0.0 |
Adolescent | 6 | 0.0 |
Adult | 10 | 0.0 |
Electroretinography | 5 | 2.0 |
Female | 20 | 0.0 |
Fluorescein Angiography | 4 | 3.0 |
Fundus Oculi | 5 | 5.0 |
Genes, Recessive | 2 | 0.0 |
Male | 16 | 0.0 |
Middle Aged | 8 | 0.0 |
*Mutation | 9 | 0.0 |
Phenotype | 9 | 0.0 |
Photoreceptors, Vertebrate/*pathology | 3 | 18.0 |
Research Support, Non-U.S. Gov't | 30 | 0.0 |
Alleles | 8 | 0.0 |
Base Sequence | 10 | 0.0 |
Gene Frequency | 2 | 0.0 |
Heterozygote | 2 | 0.0 |
Molecular Sequence Data | 9 | 0.0 |
Animals | 9 | 0.0 |
Chromosome Mapping | 5 | 0.0 |
Comparative Study | 6 | 0.0 |
Asian Continental Ancestry Group/*genetics | 2 | 0.0 |
Mutation/*genetics | 3 | 0.0 |
Aged | 8 | 0.0 |
Aged, 80 and over | 4 | 0.0 |
DNA Mutational Analysis | 13 | 0.0 |
Genotype | 10 | 0.0 |
Mutation | 8 | 0.0 |
Pedigree | 13 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 18 | 0.0 |
Adenosine Triphosphate/metabolism | 2 | 0.0 |
*Alleles | 4 | 0.0 |
Blotting, Western | 2 | 0.0 |
Cell Line | 4 | 0.0 |
DNA/chemistry/genetics | 3 | 0.0 |
Eye Diseases, Hereditary/*genetics | 2 | 10.0 |
Family Health | 2 | 0.0 |
Macular Degeneration/*genetics | 6 | 12.0 |
Protein Binding | 3 | 0.0 |
*Mutation, Missense | 2 | 0.0 |
ATP-Binding Cassette Transporters/*genetics/*metabolism | 2 | 14.0 |
Amino Acid Sequence | 5 | 0.0 |
Protein Structure, Tertiary | 3 | 0.0 |
Molecular Biology | 2 | 0.0 |
Retinitis Pigmentosa/*genetics/pathology | 2 | 8.0 |
Macular Degeneration/*genetics/pathology | 2 | 11.0 |
Polymorphism, Genetic | 6 | 0.0 |
Polymorphism, Single-Stranded Conformational | 7 | 0.0 |
Retinal Degeneration/genetics/pathology | 2 | 50.0 |
Spain | 2 | 0.0 |
Mutation, Missense | 2 | 0.0 |
Reference Values | 2 | 0.0 |
Age of Onset | 3 | 0.0 |
Child | 4 | 0.0 |
Retinal Diseases/*genetics | 3 | 9.0 |
ATP-Binding Cassette Transporters/genetics | 3 | 4.0 |
Macular Degeneration/diagnosis/*genetics | 2 | 66.0 |
Cloning, Molecular | 2 | 0.0 |
Sequence Homology, Amino Acid | 3 | 0.0 |
Child, Preschool | 2 | 0.0 |
Chromatography, High Pressure Liquid | 2 | 0.0 |
Chromosomes, Human/genetics | 2 | 4.0 |
Exons/genetics | 2 | 0.0 |
Genes, Recessive/genetics | 3 | 3.0 |
Homozygote | 2 | 0.0 |
Netherlands | 2 | 1.0 |
Case-Control Studies | 2 | 0.0 |
Genetic Predisposition to Disease/*genetics | 2 | 0.0 |
Genetic Screening | 2 | 0.0 |
Reproducibility of Results | 2 | 0.0 |
Oligonucleotide Array Sequence Analysis | 2 | 0.0 |
Variation (Genetics) | 2 | 0.0 |
Mice | 4 | 0.0 |
ATP-Binding Cassette Transporters/*genetics/metabolism | 2 | 6.0 |
Retinal Degeneration/genetics | 2 | 13.0 |
Retinitis Pigmentosa/*genetics | 2 | 1.0 |
Retinal Diseases/*genetics/pathology | 2 | 40.0 |
