Gene retinitis pigmentosa usher patients drugs. Medical search. Frequent questions

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Anatomy15

Photoreceptor Cells, Vertebrate Retina Fundus Oculi Photoreceptor Cells Retinal Rod Photoreceptor Cells Retinal Cone Photoreceptor Cells X Chromosome Photoreceptor Connecting Cilium Retinal Photoreceptor Cell Outer Segment Fovea Centralis Macula Lutea Cilia Rod Cell Outer Segment Retinal Bipolar Cells Retinal Pigment Epithelium

Organisms1

Rats, Transgenic

Diseases26

Retinitis Pigmentosa Usher Syndromes Cytomegalovirus Retinitis Retinitis Retinal Degeneration Genetic Diseases, X-Linked Night Blindness Blindness Eye Diseases, Hereditary Syndrome Hearing Loss, Sensorineural Laurence-Moon Syndrome Retinal Diseases Vision Disorders Leber Congenital Amaurosis Deafness Disease Models, Animal Retinal Dysplasia Optic Atrophy, Hereditary, Leber Ataxia Eye Infections, Viral Bardet-Biedl Syndrome Retinal Dystrophies Vision, Low Optic Atrophies, Hereditary Hearing Loss

Chemicals and Drugs18

Eye Proteins Rhodopsin Peripherins Cyclic Nucleotide Phosphodiesterases, Type 6 Rod Opsins IMP Dehydrogenase Carbonic Anhydrase IV Ribonucleoprotein, U4-U6 Small Nuclear Tetraspanins Intermediate Filament Proteins Opsins cis-trans-Isomerases Codon, Nonsense Carrier Proteins Membrane Proteins Foscarnet Nerve Tissue Proteins Arrestin

Analytical, Diagnostic and Therapeutic Techniques and Equipment17

Electroretinography Pedigree Visual Acuity DNA Mutational Analysis Visual Field Tests Tomography, Optical Coherence Fluorescein Angiography Chromosome Mapping Disease Models, Animal Sequence Analysis, DNA Vision Tests Polymerase Chain Reaction Ophthalmoscopy Visual Prosthesis Ophthalmoscopes Electrooculography Genetic Testing

Psychiatry and Psychology5

Visual Acuity Visual Fields Sensory Thresholds Phosphenes Vision, Ocular

Phenomena and Processes30

Genes, Dominant Genes, Recessive Dark Adaptation Visual Acuity Visual Fields Mutation Genetic Linkage Consanguinity X Chromosome Exons Mutation, Missense Homozygote Phenotype Polymorphism, Single-Stranded Conformational Lod Score Frameshift Mutation Genetic Heterogeneity Amino Acid Sequence Heterozygote Base Sequence Genes, X-Linked Codon, Nonsense Phosphenes Vision, Ocular Genotype Point Mutation Light Haplotypes RNA Splicing Microsatellite Repeats

Information Science3

Molecular Sequence Data Amino Acid Sequence Base 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

Retinitis Pigmentosa Usher Syndromes Cytomegalovirus Retinitis Electroretinography Eye Proteins Rhodopsin Retinitis Retinal Degeneration Photoreceptor Cells, Vertebrate Pedigree Genes, Dominant Genes, Recessive Retina Peripherins Fundus Oculi Genetic Diseases, X-Linked Dark Adaptation Visual Acuity Photoreceptor Cells Cyclic Nucleotide Phosphodiesterases, Type 6 Visual Fields Retinal Rod Photoreceptor Cells Mutation Retinal Cone Photoreceptor Cells DNA Mutational Analysis Genetic Linkage Night Blindness Consanguinity Blindness Rod Opsins Visual Field Tests X Chromosome Exons Mutation, Missense Homozygote Molecular Sequence Data Eye Diseases, Hereditary Syndrome Tomography, Optical Coherence Fluorescein Angiography IMP Dehydrogenase Photoreceptor Connecting Cilium Hearing Loss, Sensorineural Laurence-Moon Syndrome Retinal Diseases Carbonic Anhydrase IV Phenotype Chromosome Mapping Vision Disorders Leber Congenital Amaurosis Ribonucleoprotein, U4-U6 Small Nuclear Polymorphism, Single-Stranded Conformational Retinal Photoreceptor Cell Outer Segment Tetraspanins Fovea Centralis Lod Score Frameshift Mutation Intermediate Filament Proteins Genetic Heterogeneity Deafness Sensory Thresholds Opsins Amino Acid Sequence Disease Models, Animal Heterozygote Base Sequence cis-trans-Isomerases Genes, X-Linked Retinal Dysplasia Macula Lutea Codon, Nonsense Optic Atrophy, Hereditary, Leber Ataxia Phosphenes Eye Infections, Viral Sequence Analysis, DNA Cilia Vision Tests Vision, Ocular Bardet-Biedl Syndrome Retinal Dystrophies Genotype Polymerase Chain Reaction Ophthalmoscopy Vision, Low Point Mutation Carrier Proteins Rats, Transgenic Visual Prosthesis Light Rod Cell Outer Segment Ophthalmoscopes Electrooculography Membrane Proteins Optic Atrophies, Hereditary Haplotypes Foscarnet RNA Splicing Microsatellite Repeats Nerve Tissue Proteins

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