Autosomal genetic muscular dystrophies limb girdle. Medical search. Frequent questions

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Anatomy27

Muscle, Skeletal Myoblasts Muscle Fibers, Skeletal Limb Buds Scapula Extremities Shoulder Muscles Sarcolemma Chromosomes, Human, Pair 4 X Chromosome Animal Fins Forelimb Pelvis Clavicle Diaphragm Hindlimb Satellite Cells, Skeletal Muscle Muscle Cells Myoblasts, Skeletal Lower Extremity Arm Leg Pectoralis Muscles Cells, Cultured Nuclear Envelope Sacroiliac Joint

Organisms6

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

Diseases36

Muscular Dystrophies Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Pelvic Girdle Pain Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Muscular Diseases Distal Myopathies Muscle Weakness Fuchs' Endothelial Dystrophy Retinal Dystrophies Myositis, Inclusion Body Neuromuscular Diseases Pelvic Pain Neuroaxonal Dystrophies Disease Models, Animal Sarcoglycanopathies Walker-Warburg Syndrome Cardiomyopathies Limb Deformities, Congenital Reflex Sympathetic Dystrophy Phantom Limb Vitelliform Macular Dystrophy Myositis Brachial Plexus Neuritis Muscular Atrophy Syndrome Cardiomyopathy, Dilated Myotonic Disorders Retinal Degeneration Retinitis Pigmentosa Intellectual Disability

Chemicals and Drugs34

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment17

Pedigree DNA Mutational Analysis Heterozygote Detection Biopsy Immunohistochemistry Disease Models, Animal Limb Salvage Genetic Therapy Muscle Strength Electromyography Chromosome Mapping Electroretinography Prenatal Diagnosis Polymerase Chain Reaction Cineradiography Genetic Testing Blotting, Western

Psychiatry and Psychology2

Phantom Limb Intellectual Disability

Phenomena and Processes28

Mutation Mutation, Missense Phenotype Chromosomes, Human, Pair 4 Exons X Chromosome Genes, Recessive Genetic Linkage Regeneration Muscle Development Consanguinity Genes, Dominant Muscle Strength Heterozygote Homozygote Base Sequence Trinucleotide Repeat Expansion Glycosylation Biomechanical Phenomena Frameshift Mutation Muscle Contraction Codon, Nonsense Locomotion Genotype Amino Acid Sequence Time Factors Gene Deletion Genetic Markers

Disciplines and Occupations3

Immunohistochemistry Paleontology Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Fossils Paleontology

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care3

Age of Onset Genetic Counseling Genetic Testing

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

Muscular Dystrophies Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Sarcoglycans Dystrophin Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Dystroglycans Pelvic Girdle Pain Mice, Inbred mdx Muscular Dystrophy, Emery-Dreifuss Caveolin 3 Muscle, Skeletal Muscle Proteins Calpain Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Connectin Utrophin Muscular Diseases Distal Myopathies Creatine Kinase Pedigree Myoblasts Muscle Fibers, Skeletal Muscle Weakness Mutation Fuchs' Endothelial Dystrophy Cytoskeletal Proteins Mutation, Missense Phenotype Caveolins Thymopoietins Limb Buds Retinal Dystrophies Collagen Type VI Membrane Proteins Scapula Extremities Myositis, Inclusion Body Shoulder Muscles DNA Mutational Analysis Dystrophin-Associated Proteins Sarcolemma Heterozygote Detection Age of Onset Laminin Biopsy Neuromuscular Diseases Pelvic Pain Chromosomes, Human, Pair 4 Lamin Type A Exons Dystrophin-Associated Protein Complex Poly(A)-Binding Protein II Immunohistochemistry X Chromosome Animal Fins Genes, Recessive Neuroaxonal Dystrophies Disease Models, Animal Sarcoglycanopathies Genetic Linkage Walker-Warburg Syndrome Regeneration Forelimb Limb Salvage Pelvis Cardiomyopathies Clavicle Limb Deformities, Congenital Plectin Muscle Development Genetic Therapy Molecular Sequence Data Consanguinity Genes, Dominant Reflex Sympathetic Dystrophy Muscle Strength Diaphragm Hindlimb Phantom Limb Heterozygote Electromyography Vitelliform Macular Dystrophy Mice, Inbred C57BL Homozygote Chromosome Mapping Myositis Myostatin Brachial Plexus Neuritis Fossils Satellite Cells, Skeletal Muscle Lamins Base Sequence Dependovirus Mice, Transgenic Muscular Atrophy

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