Vmd2 mutations genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy15

Fundus Oculi Photoreceptor Cells, Vertebrate Retina Pigment Epithelium of Eye Photoreceptor Cells Retinal Pigment Epithelium Retinal Rod Photoreceptor Cells Retinal Cone Photoreceptor Cells Muscle, Skeletal Rod Cell Outer Segment Cell Line Chromosomes, Human, Pair 19 X Chromosome Myoblasts Muscles

Organisms6

Mice, Inbred mdx Rats, Mutant Strains Mice, Inbred C57BL Mice, Knockout Escherichia coli Mice, Transgenic

Diseases41

Retinal Dystrophies Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Muscular Dystrophy, Duchenne Retinitis Pigmentosa Corneal Dystrophies, Hereditary Muscular Dystrophy, Animal Eye Diseases, Hereditary Retinal Diseases Fuchs' Endothelial Dystrophy Vitelliform Macular Dystrophy Laurence-Moon Syndrome Blindness Muscular Dystrophy, Facioscapulohumeral Macular Degeneration Microphthalmos Bardet-Biedl Syndrome Night Blindness Syndrome Alstrom Syndrome Muscular Dystrophy, Emery-Dreifuss Optic Atrophy, Hereditary, Leber Usher Syndromes Optic Atrophies, Hereditary Neuroaxonal Dystrophies Choroid Diseases Kidney Diseases, Cystic Optic Disk Drusen Abnormalities, Multiple Intellectual Disability Muscular Dystrophy, Oculopharyngeal Reflex Sympathetic Dystrophy Vision Disorders Disease Models, Animal Myotonic Disorders Genetic Predisposition to Disease Corneal Dystrophy, Juvenile Epithelial of Meesmann Genetic Diseases, X-Linked Muscular Diseases

Chemicals and Drugs34

Eye Proteins cis-trans-Isomerases Peripherins Dystrophin Codon, Nonsense Chloride Channels Sarcoglycans Membrane Proteins Lipofuscin Carrier Proteins Proteins Rhodopsin Nerve Tissue Proteins Dystroglycans Intermediate Filament Proteins ATP-Binding Cassette Transporters Utrophin Rod Opsins Guanylate Cyclase DNA Primers DNA Receptor Protein-Tyrosine Kinases Codon Thymopoietins DNA-Binding Proteins Transcription Factors Mutant Proteins Collagen Type VI RNA, Messenger Muscle Proteins Nuclear Proteins Lamin Type A Cytoskeletal Proteins Collagen Type VIII

Analytical, Diagnostic and Therapeutic Techniques and Equipment23

Electroretinography Pedigree DNA Mutational Analysis Visual Acuity Chromosome Mapping Polymerase Chain Reaction Amino Acid Substitution Fluorescein Angiography Sequence Analysis, DNA Genetic Testing Heteroduplex Analysis Tomography, Optical Coherence Visual Field Tests Ophthalmoscopy Disease Models, Animal Mutagenesis, Site-Directed Heterozygote Detection Models, Molecular Sequence Alignment Cloning, Molecular Genetic Complementation Test Models, Genetic Transfection

Psychiatry and Psychology4

Visual Acuity Visual Fields Intellectual Disability Vision, Ocular

Phenomena and Processes51

Mutation, Missense Point Mutation Mutation Genes, Recessive Consanguinity Frameshift Mutation Genes, Dominant Exons Codon, Nonsense Phenotype Heterozygote Base Sequence Germ-Line Mutation Polymorphism, Single-Stranded Conformational Homozygote Dark Adaptation Visual Acuity Amino Acid Sequence Genetic Linkage Amino Acid Substitution Genotype Exome Mutation Rate Visual Fields Alleles Lod Score Protein Structure, Tertiary Haplotypes Mutagenesis Sequence Deletion Polymorphism, Single Nucleotide Chromosomes, Human, Pair 19 Gene Deletion Founder Effect Sequence Homology, Amino Acid Vision, Ocular Codon Suppression, Genetic Binding Sites Light X Chromosome Fluorescence Trinucleotide Repeat Expansion Protein Binding Genetic Predisposition to Disease Transfection Introns Genes, p53 Polymorphism, Genetic Microsatellite Repeats Plasmids

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care3

Age of Onset Genetic Testing Family Health

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

Retinal Dystrophies Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Muscular Dystrophy, Duchenne Mutation, Missense Point Mutation Retinitis Pigmentosa Eye Proteins Mutation Electroretinography Corneal Dystrophies, Hereditary Pedigree cis-trans-Isomerases Fundus Oculi Muscular Dystrophy, Animal Eye Diseases, Hereditary Genes, Recessive Consanguinity Retinal Diseases DNA Mutational Analysis Frameshift Mutation Fuchs' Endothelial Dystrophy Vitelliform Macular Dystrophy Laurence-Moon Syndrome Photoreceptor Cells, Vertebrate Retina Peripherins Genes, Dominant Pigment Epithelium of Eye Blindness Exons Dystrophin Muscular Dystrophy, Facioscapulohumeral Codon, Nonsense Macular Degeneration Phenotype Molecular Sequence Data Microphthalmos Bardet-Biedl Syndrome Heterozygote Night Blindness Syndrome Base Sequence Photoreceptor Cells Germ-Line Mutation Polymorphism, Single-Stranded Conformational Alstrom Syndrome Homozygote Dark Adaptation Visual Acuity Chromosome Mapping Chloride Channels Retinal Pigment Epithelium Polymerase Chain Reaction Muscular Dystrophy, Emery-Dreifuss Amino Acid Sequence Optic Atrophy, Hereditary, Leber Usher Syndromes Mice, Inbred mdx Age of Onset Genetic Linkage Amino Acid Substitution Genotype Retinal Rod Photoreceptor Cells Fluorescein Angiography Optic Atrophies, Hereditary Sequence Analysis, DNA Genetic Testing Exome Retinal Cone Photoreceptor Cells Neuroaxonal Dystrophies Choroid Diseases Sarcoglycans Kidney Diseases, Cystic Heteroduplex Analysis Optic Disk Drusen Rats, Mutant Strains Membrane Proteins Mutation Rate Abnormalities, Multiple Lipofuscin Carrier Proteins Visual Fields Proteins Rhodopsin Alleles Nerve Tissue Proteins Tomography, Optical Coherence Lod Score Dystroglycans Intellectual Disability Muscular Dystrophy, Oculopharyngeal Visual Field Tests Muscle, Skeletal Reflex Sympathetic Dystrophy Intermediate Filament Proteins Vision Disorders Ophthalmoscopy

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