Mutations causing retinitis pigmentosa. Medical search. Frequent questions

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Anatomy19

Photoreceptor Cells, Vertebrate Retina Fundus Oculi Photoreceptor Cells Retinal Rod Photoreceptor Cells Retinal Cone Photoreceptor Cells X Chromosome Retinal Photoreceptor Cell Outer Segment Fovea Centralis Photoreceptor Connecting Cilium Macula Lutea Cilia Rod Cell Outer Segment Chromosomes, Human, Pair 19 Retinal Pigment Epithelium Retinal Bipolar Cells Pigment Epithelium of Eye Chromosomes, Human, X Retinal Photoreceptor Cell Inner Segment

Organisms4

Rats, Transgenic Mice, Mutant Strains Dependovirus Animals, Genetically Modified

Diseases26

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

Chemicals and Drugs23

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment19

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

Psychiatry and Psychology6

Visual Acuity Visual Fields Sensory Thresholds Phosphenes Vision, Ocular Family

Phenomena and Processes41

Genes, Dominant Mutation Mutation, Missense Genes, Recessive Point Mutation Dark Adaptation Visual Acuity Visual Fields Genetic Linkage Frameshift Mutation Exons Consanguinity X Chromosome Homozygote Polymorphism, Single-Stranded Conformational Base Sequence Heterozygote Phenotype Amino Acid Sequence Codon, Nonsense Lod Score Genotype Amino Acid Substitution Germ-Line Mutation Genes, X-Linked Alleles Phosphenes RNA Splicing Vision, Ocular Microsatellite Repeats Genetic Heterogeneity Light Introns Sequence Deletion Chromosomes, Human, Pair 19 Mutation Rate Penetrance Exome Sequence Homology, Amino Acid Genetic Markers Chromosomes, Human, X

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups1

Asian Continental Ancestry Group

Health Care2

Genetic Testing Age of Onset

Geographicals1

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care Geographicals

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

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