Dominant myotonic dystrophy. Medical search. Frequent questions

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Anatomy5

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

Organisms1

Mice, Inbred mdx

Diseases17

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

Chemicals and Drugs6

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment1

Phenomena and Processes17

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

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

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