Recessive muscular dystrophy duchenne. Medical search. Frequent questions

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Anatomy9

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

Organisms3

Mice, Inbred mdx Mice, Inbred C57BL Dependovirus

Diseases22

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Fuchs' Endothelial Dystrophy Retinal Dystrophies Neuromuscular Diseases Muscular Diseases Disease Models, Animal Cardiomyopathies Syndrome Neuroaxonal Dystrophies Walker-Warburg Syndrome Sarcoglycanopathies Muscle Weakness Myositis Retinitis Pigmentosa

Chemicals and Drugs23

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

Pedigree Heterozygote Detection Disease Models, Animal Chromosome Mapping DNA Mutational Analysis Genetic Therapy Muscle Strength Prenatal Diagnosis Polymerase Chain Reaction

Phenomena and Processes18

Genes, Recessive Mutation Exons X Chromosome Consanguinity Phenotype Genetic Linkage Chromosomes, Human, Pair 4 Heterozygote Homozygote Regeneration Muscle Strength Genes, Dominant Base Sequence Muscle Development Mutation, Missense Codon, Nonsense Frameshift Mutation

Disciplines and Occupations1

Genetic Counseling

Information Science2

Molecular Sequence Data Base Sequence

Health Care1

Genetic Counseling

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

Sarcoglycans Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Cytoskeletal Proteins Dystrophin Membrane Glycoproteins Mice, Inbred mdx Genes, Recessive Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Utrophin Dystroglycans Corneal Dystrophies, Hereditary Muscle, Skeletal Muscular Dystrophy, Oculopharyngeal Pedigree Heterozygote Detection Fuchs' Endothelial Dystrophy Dystrophin-Associated Proteins Mutation Sarcolemma Thymopoietins Exons Creatine Kinase Retinal Dystrophies X Chromosome Collagen Type VI Muscle Fibers, Skeletal Muscles Consanguinity Myoblasts Muscle Proteins Phenotype Genetic Linkage Dystrophin-Associated Protein Complex Neuromuscular Diseases Caveolin 3 Muscular Diseases Laminin Disease Models, Animal Chromosomes, Human, Pair 4 Heterozygote Lamin Type A Cardiomyopathies Chromosome Mapping DNA Mutational Analysis Genetic Therapy Poly(A)-Binding Protein II Homozygote Molecular Sequence Data Diaphragm Syndrome Regeneration Muscle Strength Neuroaxonal Dystrophies Genes, Dominant Membrane Proteins Walker-Warburg Syndrome Mice, Inbred C57BL Base Sequence Calpain Sarcoglycanopathies Muscle Weakness Muscle Development Pregnenediones Mutation, Missense Prenatal Diagnosis Codon, Nonsense Plectin Genetic Counseling Dependovirus Frameshift Mutation Satellite Cells, Skeletal Muscle Myostatin Morpholinos Polymerase Chain Reaction Myositis Retinitis Pigmentosa

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