Duchenne myotonic dystrophy. Medical search. Frequent questions

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Anatomy8

Muscle, Skeletal Chromosomes, Human, Pair 19 Myoblasts Muscles Muscle Fibers, Skeletal Chromosomes, Human, 19-20 X Chromosome Sarcolemma

Organisms1

Mice, Inbred mdx

Diseases18

Myotonic Dystrophy Muscular Dystrophy, Duchenne Muscular Dystrophies Myotonic Disorders Muscular Dystrophy, Animal Corneal Dystrophies, Hereditary Myotonia Muscular Dystrophy, Facioscapulohumeral Fuchs' Endothelial Dystrophy Retinal Dystrophies Neuromuscular Diseases Myotonia Congenita Muscular Dystrophy, Emery-Dreifuss Lens Diseases Neuroaxonal Dystrophies Muscle Weakness Disease Models, Animal Anticipation, Genetic

Chemicals and Drugs10

Dystrophin Utrophin RNA-Binding Proteins Protein-Serine-Threonine Kinases Sarcoglycans Dystrophin-Associated Proteins Dystroglycans RNA 3' Untranslated Regions DNA

Analytical, Diagnostic and Therapeutic Techniques and Equipment5

Pedigree Heterozygote Detection Disease Models, Animal Polymerase Chain Reaction Prenatal Diagnosis

Phenomena and Processes17

Trinucleotide Repeat Expansion Trinucleotide Repeats DNA Repeat Expansion Chromosomes, Human, Pair 19 Exons Alternative Splicing Repetitive Sequences, Nucleic Acid Mutation Base Sequence Chromosomes, Human, 19-20 Genetic Linkage RNA Splicing Phenotype Alleles X Chromosome 3' Untranslated Regions Anticipation, Genetic

Information Science2

Base Sequence Molecular Sequence Data

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Information Science

Myotonic Dystrophy Muscular Dystrophy, Duchenne Muscular Dystrophies Myotonic Disorders Dystrophin Trinucleotide Repeat Expansion Muscular Dystrophy, Animal Mice, Inbred mdx Trinucleotide Repeats Corneal Dystrophies, Hereditary Myotonia Muscular Dystrophy, Facioscapulohumeral Utrophin Muscle, Skeletal Fuchs' Endothelial Dystrophy RNA-Binding Proteins Pedigree Protein-Serine-Threonine Kinases DNA Repeat Expansion Retinal Dystrophies Chromosomes, Human, Pair 19 Heterozygote Detection Myoblasts Exons Muscles Sarcoglycans Dystrophin-Associated Proteins Alternative Splicing Neuromuscular Diseases Repetitive Sequences, Nucleic Acid Mutation Muscle Fibers, Skeletal Dystroglycans Myotonia Congenita Muscular Dystrophy, Emery-Dreifuss Base Sequence Lens Diseases Chromosomes, Human, 19-20 Neuroaxonal Dystrophies Muscle Weakness Molecular Sequence Data RNA Genetic Linkage RNA Splicing Phenotype Disease Models, Animal Alleles X Chromosome Polymerase Chain Reaction Sarcolemma 3' Untranslated Regions DNA Prenatal Diagnosis Anticipation, Genetic

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