Mutation myotonic dystrophy. Medical search. Frequent questions

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Anatomy6

Chromosomes, Human, Pair 19 Muscle, Skeletal Myoblasts Chromosomes, Human, 19-20 Muscles Cell Line

Organisms1

Mice, Inbred mdx

Diseases17

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

Chemicals and Drugs9

RNA-Binding Proteins Protein-Serine-Threonine Kinases Dystrophin RNA DNA Sarcoglycans DNA Primers RNA, Messenger 3' Untranslated Regions

Analytical, Diagnostic and Therapeutic Techniques and Equipment7

Pedigree Polymerase Chain Reaction DNA Mutational Analysis Genetic Testing Heterozygote Detection Chromosome Mapping Amino Acid Substitution

Phenomena and Processes29

Trinucleotide Repeat Expansion Point Mutation Trinucleotide Repeats Mutation, Missense Mutation DNA Repeat Expansion Chromosomes, Human, Pair 19 Frameshift Mutation Base Sequence Exons Alleles Repetitive Sequences, Nucleic Acid Alternative Splicing Germ-Line Mutation Heterozygote Genes, Dominant Phenotype Genetic Linkage RNA Splicing Founder Effect Chromosomes, Human, 19-20 Amino Acid Sequence Mutation Rate 3' Untranslated Regions Genotype Genes, Recessive Anticipation, Genetic Amino Acid Substitution Mutagenesis

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care2

Genetic Testing Age of Onset

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

Myotonic Dystrophy Muscular Dystrophies Myotonic Disorders Trinucleotide Repeat Expansion Muscular Dystrophy, Duchenne Point Mutation Corneal Dystrophies, Hereditary Trinucleotide Repeats Mutation, Missense Mutation Myotonia Muscular Dystrophy, Animal Pedigree Muscular Dystrophy, Facioscapulohumeral Fuchs' Endothelial Dystrophy RNA-Binding Proteins Protein-Serine-Threonine Kinases DNA Repeat Expansion Retinal Dystrophies Chromosomes, Human, Pair 19 Frameshift Mutation Muscle, Skeletal Base Sequence Dystrophin Exons Molecular Sequence Data Alleles Repetitive Sequences, Nucleic Acid Alternative Splicing Germ-Line Mutation Polymerase Chain Reaction DNA Mutational Analysis Myotonia Congenita Heterozygote Myoblasts Genes, Dominant Phenotype Muscular Dystrophy, Emery-Dreifuss Mice, Inbred mdx RNA Genetic Linkage RNA Splicing Lens Diseases Founder Effect DNA Genetic Testing Heterozygote Detection Chromosomes, Human, 19-20 Neuroaxonal Dystrophies Sarcoglycans Amino Acid Sequence Muscles DNA Primers RNA, Messenger Chromosome Mapping Age of Onset Mutation Rate 3' Untranslated Regions Genotype Neuromuscular Diseases Genes, Recessive Muscle Weakness Anticipation, Genetic Amino Acid Substitution Cell Line Mutagenesis

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