Weakness myotonic dystrophy. Medical search. Frequent questions

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Anatomy6

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

Organisms1

Mice, Inbred mdx

Diseases19

Myotonic Dystrophy Muscular Dystrophies Myotonic Disorders Muscle Weakness Muscular Dystrophy, Duchenne Corneal Dystrophies, Hereditary Myotonia Muscular Dystrophy, Animal Muscular Dystrophy, Facioscapulohumeral Fuchs' Endothelial Dystrophy Retinal Dystrophies Neuromuscular Diseases Myotonia Congenita Muscular Dystrophy, Emery-Dreifuss Muscular Diseases Lens Diseases Neuroaxonal Dystrophies Anticipation, Genetic Muscular Dystrophy, Oculopharyngeal

Chemicals and Drugs6

RNA-Binding Proteins Protein-Serine-Threonine Kinases Dystrophin RNA Sarcoglycans 3' Untranslated Regions

Analytical, Diagnostic and Therapeutic Techniques and Equipment2

Pedigree Electromyography

Phenomena and Processes13

Trinucleotide Repeat Expansion Trinucleotide Repeats DNA Repeat Expansion Chromosomes, Human, Pair 19 Repetitive Sequences, Nucleic Acid Alternative Splicing Mutation Base Sequence Chromosomes, Human, 19-20 Exons Phenotype 3' Untranslated Regions Anticipation, Genetic

Information Science2

Base Sequence Molecular Sequence Data

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

Myotonic Dystrophy Muscular Dystrophies Myotonic Disorders Muscle Weakness Trinucleotide Repeat Expansion Muscular Dystrophy, Duchenne Trinucleotide Repeats Corneal Dystrophies, Hereditary Myotonia Muscular Dystrophy, Animal Muscular Dystrophy, Facioscapulohumeral Fuchs' Endothelial Dystrophy RNA-Binding Proteins Muscle, Skeletal Protein-Serine-Threonine Kinases DNA Repeat Expansion Retinal Dystrophies Chromosomes, Human, Pair 19 Dystrophin Pedigree Repetitive Sequences, Nucleic Acid Neuromuscular Diseases Alternative Splicing Myoblasts Myotonia Congenita Muscular Dystrophy, Emery-Dreifuss Mice, Inbred mdx Mutation Muscular Diseases Lens Diseases Base Sequence Muscles Chromosomes, Human, 19-20 Neuroaxonal Dystrophies RNA Sarcoglycans Exons Electromyography Molecular Sequence Data Muscle Fibers, Skeletal Phenotype 3' Untranslated Regions Anticipation, Genetic Muscular Dystrophy, Oculopharyngeal

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