Diseases muscular dystrophies. Medical search. Frequent questions

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Anatomy18

Muscle, Skeletal Sarcolemma Myoblasts Muscle Fibers, Skeletal Muscles Chromosomes, Human, Pair 4 X Chromosome Diaphragm Satellite Cells, Skeletal Muscle Muscle Cells Myoblasts, Skeletal Nuclear Envelope Cells, Cultured Myocardium Neuromuscular Junction Fundus Oculi Sarcomeres Costameres

Organisms7

Mice, Inbred mdx Mice, Inbred C57BL Dependovirus Mice, Transgenic Mice, Knockout Mice, Mutant Strains Dogs

Diseases39

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Fuchs' Endothelial Dystrophy Retinal Dystrophies Muscular Diseases Neuromuscular Diseases Neuroaxonal Dystrophies Disease Models, Animal Sarcoglycanopathies Walker-Warburg Syndrome Cardiomyopathies Reflex Sympathetic Dystrophy Muscle Weakness Vitelliform Macular Dystrophy Myositis Cardiomyopathy, Dilated Muscular Atrophy Myotonic Disorders Syndrome Retinal Degeneration Retinitis Pigmentosa Distal Myopathies Intellectual Disability Epidermolysis Bullosa Simplex Chromosome Deletion Fibrosis Contracture Scoliosis Corneal Dystrophy, Juvenile Epithelial of Meesmann Myoglobinuria Disease Progression Lipodystrophy

Chemicals and Drugs43

Dystrophin Sarcoglycans Dystroglycans Utrophin Thymopoietins Collagen Type VI Dystrophin-Associated Proteins Creatine Kinase Muscle Proteins Lamin Type A Dystrophin-Associated Protein Complex Laminin Caveolin 3 Poly(A)-Binding Protein II Cytoskeletal Proteins Calpain Plectin Connectin Membrane Proteins Myostatin Lamins Creatine Kinase, MM Form Mannosyltransferases N-Acetylglucosaminyltransferases Poly(A)-Binding Protein I Membrane Glycoproteins Morpholinos Oxepins Integrin alpha Chains Codon, Nonsense Pregnenediones Evans Blue Genetic Markers Caveolins Cardiotoxins DNA RNA, Messenger Nitric Oxide Synthase Type I Glycosyltransferases Oligoribonucleotides, Antisense Collagen Type VIII Glycerol Kinase Oligonucleotides, Antisense

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

Pedigree Heterozygote Detection Disease Models, Animal Genetic Therapy DNA Mutational Analysis Muscle Strength Chromosome Mapping Immunohistochemistry Electroretinography Biopsy Prenatal Diagnosis Polymerase Chain Reaction Genetic Testing Blotting, Western Fluorescent Antibody Technique

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes36

Chromosomes, Human, Pair 4 Exons Mutation X Chromosome Phenotype Genetic Linkage Genes, Recessive Consanguinity Muscle Development Regeneration Muscle Strength Heterozygote Genes, Dominant Base Sequence Mutation, Missense Trinucleotide Repeat Expansion Homozygote Glycosylation Frameshift Mutation Codon, Nonsense Gene Deletion Genetic Markers Amino Acid Sequence Muscle Contraction Sequence Deletion Gene Expression Regulation Point Mutation Chromosome Deletion Genetic Vectors Genotype Tandem Repeat Sequences Lod Score Transgenes Haplotypes Founder Effect Alleles

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Humanities1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care3

Genetic Counseling Genetic Testing Age of Onset

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

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Dystrophin Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Mice, Inbred mdx Muscular Dystrophy, Emery-Dreifuss Sarcoglycans Corneal Dystrophies, Hereditary Dystroglycans Muscular Dystrophy, Oculopharyngeal Utrophin Muscle, Skeletal Fuchs' Endothelial Dystrophy Thymopoietins Retinal Dystrophies Collagen Type VI Pedigree Dystrophin-Associated Proteins Sarcolemma Heterozygote Detection Creatine Kinase Muscle Proteins Myoblasts Muscle Fibers, Skeletal Muscles Chromosomes, Human, Pair 4 Lamin Type A Dystrophin-Associated Protein Complex Laminin Exons Caveolin 3 Poly(A)-Binding Protein II Mutation Muscular Diseases X Chromosome Neuromuscular Diseases Phenotype Cytoskeletal Proteins Neuroaxonal Dystrophies Disease Models, Animal Sarcoglycanopathies Walker-Warburg Syndrome Genetic Linkage Calpain Cardiomyopathies Genes, Recessive Plectin Genetic Therapy Consanguinity Connectin Muscle Development Regeneration Reflex Sympathetic Dystrophy Membrane Proteins Muscle Weakness Diaphragm DNA Mutational Analysis Muscle Strength Vitelliform Macular Dystrophy Molecular Sequence Data Heterozygote Chromosome Mapping Myositis Myostatin Mice, Inbred C57BL Genes, Dominant Lamins Satellite Cells, Skeletal Muscle Dependovirus Base Sequence Mutation, Missense Immunohistochemistry Cardiomyopathy, Dilated Electroretinography Mice, Transgenic Muscular Atrophy Trinucleotide Repeat Expansion Muscle Cells Myotonic Disorders Homozygote Glycosylation Myoblasts, Skeletal Creatine Kinase, MM Form Mannosyltransferases Biopsy N-Acetylglucosaminyltransferases Prenatal Diagnosis Mice, Knockout Syndrome Retinal Degeneration Poly(A)-Binding Protein I Membrane Glycoproteins Morpholinos Genetic Counseling Polymerase Chain Reaction Oxepins Frameshift Mutation

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