Mutations corneal dystrophy juvenile epithelial of meesmann. Medical search. Frequent questions

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Anatomy6

Cornea Descemet Membrane Bowman Membrane Endothelium, Corneal Corneal Stroma Chromosomes, Human, Pair 5

Diseases13

Corneal Dystrophy, Juvenile Epithelial of Meesmann Corneal Dystrophies, Hereditary Fuchs' Endothelial Dystrophy Muscular Dystrophies Myotonic Dystrophy Muscular Dystrophy, Duchenne Corneal Opacity Muscular Dystrophy, Animal Keratoconus Amyloidosis, Familial Retinal Dystrophies Muscular Dystrophy, Facioscapulohumeral Corneal Diseases

Chemicals and Drugs9

Keratin-12 Collagen Type VIII Extracellular Matrix Proteins Keratan Sulfate Dimethylallyltranstransferase Transforming Growth Factor beta Dystrophin Keratin-3 Sulfotransferases

Analytical, Diagnostic and Therapeutic Techniques and Equipment7

Pedigree DNA Mutational Analysis Keratoplasty, Penetrating Corneal Transplantation Corneal Pachymetry Polymerase Chain Reaction Amino Acid Substitution

Phenomena and Processes13

Mutation, Missense Point Mutation Mutation Frameshift Mutation Exons Heterozygote Phenotype Base Sequence Genes, Dominant Homozygote Amino Acid Substitution Genetic Linkage Chromosomes, Human, Pair 5

Information Science3

Current Procedural Terminology Base Sequence Molecular Sequence Data

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Information Science

Corneal Dystrophy, Juvenile Epithelial of Meesmann Corneal Dystrophies, Hereditary Keratin-12 Fuchs' Endothelial Dystrophy Muscular Dystrophies Collagen Type VIII Myotonic Dystrophy Cornea Mutation, Missense Pedigree Muscular Dystrophy, Duchenne Point Mutation Mutation Corneal Opacity Descemet Membrane Extracellular Matrix Proteins DNA Mutational Analysis Bowman Membrane Muscular Dystrophy, Animal Endothelium, Corneal Keratoplasty, Penetrating Keratoconus Keratan Sulfate Amyloidosis, Familial Frameshift Mutation Corneal Stroma Exons Heterozygote Corneal Transplantation Retinal Dystrophies Current Procedural Terminology Phenotype Corneal Pachymetry Dimethylallyltranstransferase Transforming Growth Factor beta Base Sequence Dystrophin Muscular Dystrophy, Facioscapulohumeral Corneal Diseases Keratin-3 Genes, Dominant Polymerase Chain Reaction Homozygote Molecular Sequence Data Amino Acid Substitution Sulfotransferases Genetic Linkage Chromosomes, Human, Pair 5

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