Duchenne or becker muscular dystrophy. Medical search. Frequent questions

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Anatomy11

X Chromosome Muscle, Skeletal Sarcolemma Muscles Muscle Fibers, Skeletal Myoblasts Chromosomes, Human, Pair 4 Diaphragm Satellite Cells, Skeletal Muscle Myoblasts, Skeletal Muscle Cells

Organisms5

Mice, Inbred mdx Nepeta Mice, Inbred C57BL Dependovirus Viola

Diseases26

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Cardiomyopathy, Dilated Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Chromosome Deletion Cardiomyopathies Fuchs' Endothelial Dystrophy Retinal Dystrophies Neuromuscular Diseases Muscular Diseases Disease Models, Animal Myotonia Congenita Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome Muscle Weakness Myositis Reflex Sympathetic Dystrophy Syndrome Vitelliform Macular Dystrophy

Chemicals and Drugs27

Dystrophin Utrophin Sarcoglycans Deoxyribonuclease HindIII Dystroglycans Creatine Kinase Muscle Proteins DNA Probes Cytoskeletal Proteins Dystrophin-Associated Proteins Thymopoietins Collagen Type VI DNA Dystrophin-Associated Protein Complex Caveolin 3 Laminin Lamin Type A Poly(A)-Binding Protein II Oligoribonucleotides, Antisense Codon, Nonsense Calpain Pregnenediones Membrane Proteins Plectin Myostatin Morpholinos Connectin

Analytical, Diagnostic and Therapeutic Techniques and Equipment14

Heterozygote Detection Pedigree Prenatal Diagnosis Polymerase Chain Reaction Genetic Testing DNA Mutational Analysis Blotting, Southern Immunohistochemistry Disease Models, Animal Genetic Therapy Echocardiography Muscle Strength Chromosome Mapping Biopsy

Phenomena and Processes21

Exons X Chromosome Genetic Linkage Heterozygote Phenotype Chromosome Deletion Gene Deletion Mutation Frameshift Mutation Sequence Deletion Base Sequence RNA Splicing Point Mutation Chromosomes, Human, Pair 4 Regeneration Muscle Strength Codon, Nonsense Genes, Recessive Muscle Development Consanguinity Polymorphism, Restriction Fragment Length

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science2

Molecular Sequence Data Base Sequence

Health Care2

Genetic Testing Genetic Counseling

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Health Care

Muscular Dystrophies Muscular Dystrophy, Duchenne Dystrophin Muscular Dystrophy, Animal Heterozygote Detection Utrophin Mice, Inbred mdx Sarcoglycans Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Exons Muscular Dystrophy, Facioscapulohumeral X Chromosome Muscle, Skeletal Muscular Dystrophy, Emery-Dreifuss Pedigree Deoxyribonuclease HindIII Dystroglycans Sarcolemma Cardiomyopathy, Dilated Blood Stains Creatine Kinase Corneal Dystrophies, Hereditary Muscles Prenatal Diagnosis Genetic Linkage Muscular Dystrophy, Oculopharyngeal Heterozygote Phenotype Chromosome Deletion Gene Deletion Mutation Frameshift Mutation Cardiomyopathies Muscle Proteins Polymerase Chain Reaction DNA Probes Sequence Deletion Cytoskeletal Proteins Molecular Sequence Data Fuchs' Endothelial Dystrophy Genetic Testing Dystrophin-Associated Proteins DNA Mutational Analysis Thymopoietins Base Sequence Muscle Fibers, Skeletal Retinal Dystrophies Collagen Type VI Myoblasts DNA RNA Splicing Dystrophin-Associated Protein Complex Point Mutation Blotting, Southern Immunohistochemistry Neuromuscular Diseases Caveolin 3 Laminin Muscular Diseases Disease Models, Animal Chromosomes, Human, Pair 4 Lamin Type A Genetic Counseling Poly(A)-Binding Protein II Genetic Therapy Diaphragm Myotonia Congenita Echocardiography Oligoribonucleotides, Antisense Regeneration Muscle Strength Nepeta Neuroaxonal Dystrophies Codon, Nonsense Chromosome Mapping Sarcoglycanopathies Walker-Warburg Syndrome Genes, Recessive Muscle Development Calpain Biopsy Pregnenediones Mice, Inbred C57BL Muscle Weakness Membrane Proteins Plectin Satellite Cells, Skeletal Muscle Myostatin Dependovirus Morpholinos Myositis Viola Consanguinity Connectin Reflex Sympathetic Dystrophy Myoblasts, Skeletal Polymorphism, Restriction Fragment Length Syndrome Muscle Cells

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