Myopathies genetic autosomal recessive form muscular dystrophies. Medical search. Frequent questions

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Anatomy28

Muscle, Skeletal X Chromosome Muscles Myoblasts Sarcolemma Chromosomes, Human, Pair 4 Muscle Fibers, Skeletal Myofibrils Muscle Cells Mitochondria Chromosomes, Human, Pair 2 Cells, Cultured Mitochondria, Muscle Sarcomeres Diaphragm Fundus Oculi Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 1 Cell Line Satellite Cells, Skeletal Muscle Myocardium Chromosomes, Human, Pair 5 Fibroblasts Myoblasts, Skeletal Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 10 Photoreceptor Cells, Vertebrate Nuclear Envelope

Organisms8

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

Diseases91

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Myositis Muscular Dystrophies, Limb-Girdle Muscular Diseases Myotonic Dystrophy Granulomatous Disease, Chronic Muscular Dystrophy, Facioscapulohumeral Myopathies, Structural, Congenital Distal Myopathies Spastic Paraplegia, Hereditary Syndrome Muscular Dystrophy, Emery-Dreifuss Mitochondrial Myopathies Immunologic Deficiency Syndromes Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Myositis, Inclusion Body Myopathies, Nemaline Parkinson Disease Neuromuscular Diseases Arthrogryposis Dysostoses Abnormalities, Multiple Fuchs' Endothelial Dystrophy Retinal Dystrophies Polycystic Kidney, Autosomal Recessive Hearing Loss, Sensorineural Ectodermal Dysplasia Muscle Weakness Deafness Retinitis Pigmentosa Charcot-Marie-Tooth Disease Osteogenesis Imperfecta Disease Models, Animal Myopathy, Central Core Cardiomyopathies Intellectual Disability Neuroaxonal Dystrophies Muscular Atrophy Microcephaly Walker-Warburg Syndrome Hypotrichosis Ichthyosis Retinal Degeneration Vitelliform Macular Dystrophy Sarcoglycanopathies Metabolism, Inborn Errors Ichthyosiform Erythroderma, Congenital Lipid Metabolism Disorders Eye Diseases, Hereditary Nails, Malformed Chromosome Disorders Reflex Sympathetic Dystrophy Ichthyosis, Lamellar Dwarfism Cerebellar Ataxia Osteochondrodysplasias Eye Abnormalities Myotonic Disorders Cardiomyopathy, Dilated Muscular Atrophy, Spinal Genetic Diseases, Inborn Bone Diseases, Developmental Osteopetrosis Epidermolysis Bullosa Myotonia Congenita Albinism, Oculocutaneous Contracture Night Blindness Genetic Diseases, X-Linked Microphthalmos Chromosome Deletion Foot Deformities, Congenital Muscle Hypotonia Malignant Hyperthermia Genetic Predisposition to Disease Color Vision Defects Kidney Diseases, Cystic Mitochondrial Diseases Friedreich Ataxia Hair Diseases Cutis Laxa Macular Degeneration Leber Congenital Amaurosis Cystinosis Lipodystrophy Hearing Loss Retinal Diseases Rare Diseases

Chemicals and Drugs52

Dystrophin Sarcoglycans Dystroglycans Genetic Markers Utrophin Collagen Type VI Codon, Nonsense Muscle Proteins Creatine Kinase Thymopoietins Collagen Type XI Desmin Dystrophin-Associated Proteins Lamin Type A Laminin Connectin Dystrophin-Associated Protein Complex Caveolin 3 Cytoskeletal Proteins Poly(A)-Binding Protein II Membrane Proteins Ubiquitin-Protein Ligases Calpain Plectin Hemolytic Agents Eye Proteins RNA, Messenger DNA Membrane Glycoproteins LIM Domain Proteins Myostatin alpha-Crystallin B Chain Lamins DNA Primers Mannosyltransferases N-Acetylglucosaminyltransferases Cofilin 2 Proteins Creatine Kinase, MM Form RNA Splice Sites Poly(A)-Binding Protein I Morpholinos Oxepins Nerve Tissue Proteins Codon, Terminator Extracellular Matrix Proteins Integrin alpha Chains Pregnenediones Evans Blue Myosin Heavy Chains Nuclear Proteins Ryanodine Receptor Calcium Release Channel

Analytical, Diagnostic and Therapeutic Techniques and Equipment24

Pedigree DNA Mutational Analysis Chromosome Mapping Heterozygote Detection Disease Models, Animal Biopsy Electroretinography Immunohistochemistry Genetic Testing Polymerase Chain Reaction Genetic Therapy Prenatal Diagnosis Electromyography Muscle Strength Sequence Analysis, DNA Blotting, Western Microscopy, Electron, Transmission Magnetic Resonance Imaging Crosses, Genetic Case-Control Studies Microscopy, Electron Reverse Transcriptase Polymerase Chain Reaction Fluorescent Antibody Technique Models, Genetic

Psychiatry and Psychology2

Intellectual Disability Family

Phenomena and Processes55

Genes, Recessive Consanguinity Mutation Genetic Linkage Homozygote Mutation, Missense Lod Score Phenotype Exons Heterozygote Haplotypes Base Sequence Genetic Markers Amino Acid Sequence Genes, Dominant Codon, Nonsense X Chromosome Genotype Chromosomes, Human, Pair 4 Microsatellite Repeats Frameshift Mutation Regeneration Muscle Development Alleles Founder Effect Point Mutation Polymorphism, Single-Stranded Conformational Genetic Heterogeneity Sequence Deletion Chromosomes, Human, Pair 2 Exome Gene Deletion Muscle Strength Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 1 Muscle Contraction Gene Expression Regulation Glycosylation Gene Expression Introns Chromosomes, Human, Pair 5 Polymorphism, Genetic Trinucleotide Repeat Expansion Polymorphism, Restriction Fragment Length Chromosome Deletion Alternative Splicing RNA Splice Sites Genetic Predisposition to Disease Chromosomes, Human, Pair 6 Protein Binding Sequence Homology, Amino Acid RNA Splicing Chromosomes, Human, Pair 10 Codon, Terminator Genetic Vectors

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups2

Infant, Newborn Arabs

Health Care5

Family Health Genetic Testing Age of Onset Genetic Counseling Case-Control Studies

Geographicals2

Pakistan Tunisia

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 Named Groups Health Care Geographicals

Genes, Recessive Muscular Dystrophies Muscular Dystrophy, Duchenne Pedigree Muscular Dystrophy, Animal Consanguinity Myositis Dystrophin Muscular Dystrophies, Limb-Girdle Mutation Muscular Diseases Genetic Linkage Myotonic Dystrophy DNA Mutational Analysis Granulomatous Disease, Chronic Homozygote Muscular Dystrophy, Facioscapulohumeral Myopathies, Structural, Congenital Distal Myopathies Spastic Paraplegia, Hereditary Mutation, Missense Mice, Inbred mdx Chromosome Mapping Lod Score Syndrome Muscular Dystrophy, Emery-Dreifuss Phenotype Exons Sarcoglycans Mitochondrial Myopathies Muscle, Skeletal Heterozygote Immunologic Deficiency Syndromes Corneal Dystrophies, Hereditary Haplotypes Molecular Sequence Data Dystroglycans Base Sequence Muscular Dystrophy, Oculopharyngeal Genetic Markers Utrophin Collagen Type VI Myositis, Inclusion Body Myopathies, Nemaline Amino Acid Sequence Genes, Dominant Parkinson Disease Neuromuscular Diseases Arthrogryposis Dysostoses Abnormalities, Multiple Codon, Nonsense X Chromosome Muscle Proteins Fuchs' Endothelial Dystrophy Retinal Dystrophies Creatine Kinase Heterozygote Detection Polycystic Kidney, Autosomal Recessive Muscles Thymopoietins Hearing Loss, Sensorineural Ectodermal Dysplasia Myoblasts Muscle Weakness Sarcolemma Deafness Collagen Type XI Retinitis Pigmentosa Genotype Charcot-Marie-Tooth Disease Family Health Desmin Chromosomes, Human, Pair 4 Dystrophin-Associated Proteins Osteogenesis Imperfecta Disease Models, Animal Microsatellite Repeats Muscle Fibers, Skeletal Lamin Type A Myopathy, Central Core Laminin Cardiomyopathies Frameshift Mutation Connectin Biopsy Intellectual Disability Dystrophin-Associated Protein Complex Caveolin 3 Cytoskeletal Proteins Neuroaxonal Dystrophies Muscular Atrophy Poly(A)-Binding Protein II Membrane Proteins Ubiquitin-Protein Ligases Microcephaly Walker-Warburg Syndrome Hypotrichosis Regeneration Muscle Development

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