Autosomal dominant myotonic dystrophy. Medical search. Frequent questions

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Anatomy5

Chromosomes, Human, Pair 19 Muscle, Skeletal Myoblasts Chromosomes, Human, 19-20 Muscles

Organisms2

Mice, Inbred mdx Mice, Transgenic

Diseases25

Myotonic Dystrophy Muscular Dystrophies Myotonic Disorders Muscular Dystrophy, Duchenne Polycystic Kidney, Autosomal Dominant Corneal Dystrophies, Hereditary Muscular Dystrophy, Animal Myotonia Muscular Dystrophy, Facioscapulohumeral Fuchs' Endothelial Dystrophy Retinal Dystrophies Retinitis Pigmentosa Myotonia Congenita Muscular Dystrophy, Emery-Dreifuss Cataract Optic Atrophy, Autosomal Dominant Lens Diseases Anticipation, Genetic Neuroaxonal Dystrophies Neuromuscular Diseases Syndrome Muscle Weakness Muscular Diseases Disease Models, Animal Muscular Dystrophy, Oculopharyngeal

Chemicals and Drugs11

RNA-Binding Proteins Protein-Serine-Threonine Kinases Dystrophin TRPP Cation Channels Genetic Markers RNA Sarcoglycans DNA 3' Untranslated Regions Eye Proteins RNA, Messenger

Analytical, Diagnostic and Therapeutic Techniques and Equipment8

Pedigree DNA Mutational Analysis Chromosome Mapping Polymerase Chain Reaction Genetic Testing Disease Models, Animal Electroretinography Heterozygote Detection

Phenomena and Processes24

Genes, Dominant Trinucleotide Repeat Expansion Trinucleotide Repeats Mutation Genetic Linkage Chromosomes, Human, Pair 19 DNA Repeat Expansion Phenotype Lod Score Base Sequence Exons Repetitive Sequences, Nucleic Acid Alternative Splicing Mutation, Missense Alleles Genetic Markers Heterozygote Anticipation, Genetic Haplotypes Chromosomes, Human, 19-20 Genes, Recessive RNA Splicing Founder Effect 3' Untranslated Regions

Information Science2

Base Sequence Molecular Sequence Data

Health Care2

Age of Onset Genetic Testing

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

Myotonic Dystrophy Muscular Dystrophies Genes, Dominant Myotonic Disorders Trinucleotide Repeat Expansion Pedigree Muscular Dystrophy, Duchenne Polycystic Kidney, Autosomal Dominant Trinucleotide Repeats Corneal Dystrophies, Hereditary Muscular Dystrophy, Animal Myotonia Muscular Dystrophy, Facioscapulohumeral Mutation Genetic Linkage Chromosomes, Human, Pair 19 Fuchs' Endothelial Dystrophy RNA-Binding Proteins Protein-Serine-Threonine Kinases DNA Repeat Expansion Retinal Dystrophies Muscle, Skeletal Retinitis Pigmentosa DNA Mutational Analysis Phenotype Dystrophin Lod Score Base Sequence Molecular Sequence Data Exons TRPP Cation Channels Chromosome Mapping Repetitive Sequences, Nucleic Acid Myotonia Congenita Alternative Splicing Muscular Dystrophy, Emery-Dreifuss Mutation, Missense Age of Onset Myoblasts Cataract Alleles Genetic Markers Heterozygote Optic Atrophy, Autosomal Dominant Lens Diseases Mice, Inbred mdx Anticipation, Genetic Haplotypes Polymerase Chain Reaction RNA Chromosomes, Human, 19-20 Sarcoglycans Genes, Recessive Neuroaxonal Dystrophies Muscles Genetic Testing RNA Splicing Neuromuscular Diseases Syndrome Muscle Weakness DNA Founder Effect Muscular Diseases Disease Models, Animal Electroretinography 3' Untranslated Regions Muscular Dystrophy, Oculopharyngeal Eye Proteins Heterozygote Detection RNA, Messenger Mice, Transgenic

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