Leber congenital amaurosis retinal dystrophies. Medical search. Frequent questions

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Anatomy10

Photoreceptor Connecting Cilium Photoreceptor Cells, Vertebrate Retina Fundus Oculi Retinal Cone Photoreceptor Cells Retinal Rod Photoreceptor Cells Pigment Epithelium of Eye Pupil Photoreceptor Cells Retinal Pigment Epithelium

Organisms2

Dependovirus Mice, Knockout

Diseases22

Leber Congenital Amaurosis Retinal Dystrophies Optic Atrophy, Hereditary, Leber Blindness Retinal Degeneration Optic Atrophies, Hereditary Retinitis Pigmentosa Amaurosis Fugax Eye Diseases, Hereditary Muscular Dystrophies Myotonic Dystrophy Retinal Diseases Muscular Dystrophy, Duchenne Nystagmus, Congenital Corneal Dystrophies, Hereditary Muscular Dystrophy, Animal Disease Models, Animal Night Blindness Fuchs' Endothelial Dystrophy Laurence-Moon Syndrome Muscular Dystrophy, Facioscapulohumeral Bardet-Biedl Syndrome

Chemicals and Drugs16

cis-trans-Isomerases Eye Proteins Cone Opsins Carrier Proteins Guanylate Cyclase Retinaldehyde Codon, Nonsense Proteins Nerve Tissue Proteins Membrane Proteins Receptors, Cell Surface Alcohol Oxidoreductases Peripherins Rhodopsin Dystrophin Homeodomain Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

Electroretinography Pedigree DNA Mutational Analysis Injections, Intraocular Tomography, Optical Coherence Genetic Therapy Visual Acuity Disease Models, Animal Genetic Testing Fluorescein Angiography Polymerase Chain Reaction Fluorescent Antibody Technique, Indirect Reflex, Pupillary Sequence Analysis, DNA Visual Field Tests

Psychiatry and Psychology4

Night Vision Vision, Ocular Visual Acuity Visual Fields

Phenomena and Processes21

Night Vision Mutation Consanguinity Genes, Recessive Vision, Ocular Codon, Nonsense Dark Adaptation Visual Acuity Phenotype Homozygote Exons Polymorphism, Single-Stranded Conformational Visual Fields Mutation, Missense Genotype Genetic Vectors Base Sequence Genes, Dominant Reflex, Pupillary Amino Acid Sequence Genetic Linkage

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care1

Genetic Testing

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Health Care

Leber Congenital Amaurosis Retinal Dystrophies cis-trans-Isomerases Optic Atrophy, Hereditary, Leber Blindness Retinal Degeneration Eye Proteins Optic Atrophies, Hereditary Retinitis Pigmentosa Electroretinography Photoreceptor Connecting Cilium Amaurosis Fugax Photoreceptor Cells, Vertebrate Eye Diseases, Hereditary Pedigree Night Vision DNA Mutational Analysis Muscular Dystrophies Mutation Consanguinity Retina Cone Opsins Fundus Oculi Retinal Cone Photoreceptor Cells Carrier Proteins Myotonic Dystrophy Retinal Rod Photoreceptor Cells Guanylate Cyclase Retinal Diseases Genes, Recessive Vision, Ocular Retinaldehyde Injections, Intraocular Muscular Dystrophy, Duchenne Dependovirus Tomography, Optical Coherence Codon, Nonsense Genetic Therapy Dark Adaptation Nystagmus, Congenital Pigment Epithelium of Eye Visual Acuity Corneal Dystrophies, Hereditary Phenotype Homozygote Exons Polymorphism, Single-Stranded Conformational Pupil Muscular Dystrophy, Animal Visual Fields Mutation, Missense Disease Models, Animal Proteins Genotype Molecular Sequence Data Night Blindness Nerve Tissue Proteins Genetic Vectors Photoreceptor Cells Genetic Testing Retinal Pigment Epithelium Membrane Proteins Fuchs' Endothelial Dystrophy Laurence-Moon Syndrome Fluorescein Angiography Receptors, Cell Surface Polymerase Chain Reaction Mice, Knockout Fluorescent Antibody Technique, Indirect Base Sequence Genes, Dominant Alcohol Oxidoreductases Peripherins Reflex, Pupillary Amino Acid Sequence Muscular Dystrophy, Facioscapulohumeral Sequence Analysis, DNA Rhodopsin Dystrophin Genetic Linkage Homeodomain Proteins Visual Field Tests Bardet-Biedl Syndrome

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