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

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Anatomy26

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

Organisms6

Mice, Inbred mdx Mice, Knockout Mice, Inbred C57BL Cricetinae Dependovirus Mice, Transgenic

Diseases34

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

Chemicals and Drugs31

Sarcoglycans Dystrophin Dystroglycans Dystrophin-Associated Protein Complex Cytoskeletal Proteins Caveolin 3 Muscle Proteins Calpain Dystrophin-Associated Proteins Connectin Utrophin Membrane Glycoproteins Creatine Kinase Membrane Proteins Laminin Caveolins Thymopoietins Collagen Type VI Lamin Type A Poly(A)-Binding Protein II Plectin Neoplasm Proteins Carrier Proteins Myostatin Macromolecular Substances Lamins Creatine Kinase, MM Form Mannosyltransferases N-Acetylglucosaminyltransferases Morpholinos Poly(A)-Binding Protein I

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

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

Psychiatry and Psychology1

Phenomena and Processes20

Mutation Phenotype Mutation, Missense Chromosomes, Human, Pair 4 Exons X Chromosome Genes, Recessive Genetic Linkage Regeneration Amino Acid Sequence Base Sequence Muscle Development Consanguinity Genes, Dominant Muscle Strength Heterozygote Homozygote Trinucleotide Repeat Expansion Glycosylation Biomechanical Phenomena

Disciplines and Occupations3

Immunohistochemistry Paleontology Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Fossils Paleontology

Information Science3

Molecular Sequence Data Amino Acid Sequence Base Sequence

Health Care2

Age of Onset Genetic Counseling

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

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