Lgmd muscular dystrophies. Medical search. Frequent questions

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Anatomy20

Muscle, Skeletal Sarcolemma Muscles Myoblasts Muscle Fibers, Skeletal Chromosomes, Human, Pair 4 X Chromosome Diaphragm Satellite Cells, Skeletal Muscle Muscle Cells Myoblasts, Skeletal Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 2 Nuclear Envelope Chromosomes, Human, Pair 15 Cells, Cultured Myocardium Neuromuscular Junction Fundus Oculi Sarcomeres

Organisms7

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

Diseases37

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Animal Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Fuchs' Endothelial Dystrophy Retinal Dystrophies Muscular Diseases Neuromuscular Diseases Disease Models, Animal Neuroaxonal Dystrophies 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 Disease Progression Distal Myopathies Intellectual Disability Epidermolysis Bullosa Simplex Chromosome Deletion Fibrosis Contracture Scoliosis Corneal Dystrophy, Juvenile Epithelial of Meesmann

Chemicals and Drugs41

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

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

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes40

Mutation Exons Genes, Recessive Phenotype Chromosomes, Human, Pair 4 Consanguinity Genetic Linkage X Chromosome Mutation, Missense Genes, Dominant Homozygote Muscle Development Regeneration Muscle Strength Base Sequence Heterozygote Genetic Markers Genotype Lod Score Trinucleotide Repeat Expansion Glycosylation Chromosomes, Human, Pair 5 Amino Acid Sequence Frameshift Mutation Polymorphism, Single-Stranded Conformational Codon, Nonsense Chromosomes, Human, Pair 2 Gene Deletion Muscle Contraction Alleles Chromosomes, Human, Pair 15 Sequence Deletion Gene Expression Regulation Point Mutation Chromosome Deletion Genetic Heterogeneity Genetic Vectors Exome Tandem Repeat Sequences Transgenes

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups1

American Native Continental Ancestry Group

Health Care4

Age of Onset Genetic Testing Genetic Counseling Family Health

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

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Animal Dystrophin Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Sarcoglycans Mice, Inbred mdx Muscular Dystrophy, Emery-Dreifuss Dystroglycans Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Utrophin Muscle, Skeletal Muscle Proteins Fuchs' Endothelial Dystrophy Pedigree Calpain Thymopoietins Retinal Dystrophies Collagen Type VI Caveolin 3 Sarcolemma Creatine Kinase Mutation Dystrophin-Associated Proteins Muscles Heterozygote Detection Muscular Diseases Connectin Myoblasts Exons Cytoskeletal Proteins Muscle Fibers, Skeletal Genes, Recessive Phenotype Chromosomes, Human, Pair 4 Lamin Type A Dystrophin-Associated Protein Complex Laminin Consanguinity Poly(A)-Binding Protein II Genetic Linkage X Chromosome DNA Mutational Analysis Neuromuscular Diseases Disease Models, Animal Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome Membrane Proteins Mutation, Missense Cardiomyopathies Chromosome Mapping Genes, Dominant Plectin Homozygote Molecular Sequence Data Grasshoppers Genetic Therapy Muscle Development Regeneration Reflex Sympathetic Dystrophy Muscle Weakness Age of Onset Diaphragm Muscle Strength Membrane Glycoproteins Base Sequence Vitelliform Macular Dystrophy Heterozygote Myositis Myostatin Immunohistochemistry Biopsy Mice, Inbred C57BL Lamins Satellite Cells, Skeletal Muscle Dependovirus Genetic Testing Blotting, Western Genetic Markers Genotype Cardiomyopathy, Dilated Electroretinography Lod Score Mice, Transgenic Muscular Atrophy Trinucleotide Repeat Expansion Muscle Cells Myotonic Disorders Glycosylation Myoblasts, Skeletal Creatine Kinase, MM Form Chromosomes, Human, Pair 5 Mannosyltransferases N-Acetylglucosaminyltransferases Prenatal Diagnosis Mice, Knockout

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