Congenital muscular dystrophy emery dreifuss. Medical search. Frequent questions

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Anatomy5

Muscle, Skeletal Sarcolemma Muscle Fibers, Skeletal Basement Membrane Muscles

Organisms1

Mice, Inbred mdx

Diseases19

Muscular Dystrophy, Emery-Dreifuss Muscular Dystrophies Muscular Dystrophy, Animal Muscular Dystrophy, Duchenne Walker-Warburg Syndrome Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Corneal Dystrophies, Hereditary Muscular Diseases Muscular Dystrophy, Oculopharyngeal Contracture Sclerosis Eye Abnormalities Fuchs' Endothelial Dystrophy Intellectual Disability Disease Models, Animal Retinal Dystrophies Abnormalities, Multiple

Chemicals and Drugs15

Thymopoietins Collagen Type VI Dystroglycans Laminin Dystrophin Oxepins Mannosyltransferases N-Acetylglucosaminyltransferases Sarcoglycans Utrophin Glycosyltransferases Mannose Cytoskeletal Proteins Membrane Proteins Dystrophin-Associated Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment4

Pedigree Disease Models, Animal DNA Mutational Analysis Chromosome Mapping

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes9

Glycosylation Mutation Consanguinity Phenotype Exons Genes, Recessive Homozygote Genetic Linkage Heterozygote

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes

Muscular Dystrophy, Emery-Dreifuss Thymopoietins Muscular Dystrophies Collagen Type VI Muscular Dystrophy, Animal Muscular Dystrophy, Duchenne Dystroglycans Walker-Warburg Syndrome Muscular Dystrophies, Limb-Girdle Laminin Dystrophin Oxepins Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscle, Skeletal Mannosyltransferases Mice, Inbred mdx N-Acetylglucosaminyltransferases Glycosylation Sarcoglycans Corneal Dystrophies, Hereditary Muscular Diseases Muscular Dystrophy, Oculopharyngeal Mutation Consanguinity Utrophin Pedigree Glycosyltransferases Sarcolemma Muscle Fibers, Skeletal Contracture Sclerosis Phenotype Basement Membrane Eye Abnormalities Exons Mannose Fuchs' Endothelial Dystrophy Genes, Recessive Intellectual Disability Disease Models, Animal Cytoskeletal Proteins Muscles Homozygote Genetic Linkage Retinal Dystrophies DNA Mutational Analysis Abnormalities, Multiple Chromosome Mapping Heterozygote Membrane Proteins Dystrophin-Associated Proteins

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