Myotonic dystrophy muscular dystrophy emery dreifuss. Medical search. Frequent questions

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Anatomy7

Muscle, Skeletal Myoblasts Muscles Muscle Fibers, Skeletal Chromosomes, Human, Pair 19 Sarcolemma Chromosomes, Human, Pair 4

Organisms1

Mice, Inbred mdx

Diseases18

Muscular Dystrophy, Emery-Dreifuss Myotonic Dystrophy Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Muscular Dystrophy, Facioscapulohumeral Corneal Dystrophies, Hereditary Muscular Dystrophies, Limb-Girdle Myotonic Disorders Fuchs' Endothelial Dystrophy Muscular Dystrophy, Oculopharyngeal Retinal Dystrophies Myotonia Neuroaxonal Dystrophies Neuromuscular Diseases Muscular Diseases Muscle Weakness Disease Models, Animal

Chemicals and Drugs12

Thymopoietins Dystrophin Sarcoglycans Dystroglycans Utrophin RNA-Binding Proteins Dystrophin-Associated Proteins Collagen Type VI Protein-Serine-Threonine Kinases Creatine Kinase Muscle Proteins Lamin Type A

Analytical, Diagnostic and Therapeutic Techniques and Equipment3

Pedigree Heterozygote Detection Disease Models, Animal

Phenomena and Processes12

Trinucleotide Repeat Expansion Trinucleotide Repeats Mutation Exons Chromosomes, Human, Pair 19 DNA Repeat Expansion Phenotype Genetic Linkage Alternative Splicing Base Sequence Repetitive Sequences, Nucleic Acid Chromosomes, Human, Pair 4

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

Muscular Dystrophy, Emery-Dreifuss Myotonic Dystrophy Thymopoietins Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Dystrophin Muscular Dystrophy, Facioscapulohumeral Corneal Dystrophies, Hereditary Muscular Dystrophies, Limb-Girdle Myotonic Disorders Mice, Inbred mdx Trinucleotide Repeat Expansion Sarcoglycans Muscle, Skeletal Fuchs' Endothelial Dystrophy Dystroglycans Muscular Dystrophy, Oculopharyngeal Utrophin Trinucleotide Repeats Retinal Dystrophies Pedigree Myotonia Myoblasts RNA-Binding Proteins Dystrophin-Associated Proteins Muscles Collagen Type VI Mutation Heterozygote Detection Exons Muscle Fibers, Skeletal Chromosomes, Human, Pair 19 Protein-Serine-Threonine Kinases DNA Repeat Expansion Neuroaxonal Dystrophies Neuromuscular Diseases Sarcolemma Phenotype Creatine Kinase Muscular Diseases Muscle Proteins Genetic Linkage Alternative Splicing Base Sequence Repetitive Sequences, Nucleic Acid Muscle Weakness Chromosomes, Human, Pair 4 Disease Models, Animal Lamin Type A Molecular Sequence Data

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