Dmpk proteins gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy2

Intranuclear Inclusion Bodies Cell Line

Organisms2

Mice, Transgenic Saccharomyces cerevisiae

Diseases20

Friedreich Ataxia Myotonic Dystrophy Spinocerebellar Degenerations Fragile X Syndrome Huntington Disease Spinocerebellar Ataxias Machado-Joseph Disease Heredodegenerative Disorders, Nervous System Genomic Instability Frontotemporal Dementia Anticipation, Genetic Cerebellar Ataxia Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Amyotrophic Lateral Sclerosis Neurodegenerative Diseases Myotonic Disorders Myoclonic Epilepsies, Progressive Disease Models, Animal

Chemicals and Drugs18

Fragile X Mental Retardation Protein Iron-Binding Proteins Nerve Tissue Proteins DNA Flap Endonucleases RNA-Binding Proteins Nuclear Proteins Proteins Protein-Serine-Threonine Kinases Peptides RNA, Messenger DNA Primers Receptors, Androgen DNA-Binding Proteins Genetic Markers RNA MutS Homolog 2 Protein Nucleic Acid Heteroduplexes

Analytical, Diagnostic and Therapeutic Techniques and Equipment5

Pedigree Polymerase Chain Reaction Sequence Analysis, DNA Models, Genetic Disease Models, Animal

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes30

Trinucleotide Repeat Expansion Trinucleotide Repeats DNA Repeat Expansion Alleles Mutation Repetitive Sequences, Nucleic Acid Base Sequence Genomic Instability Microsatellite Repeats Anticipation, Genetic Nucleic Acid Conformation Inverted Repeat Sequences Tandem Repeat Sequences Minisatellite Repeats Chromosome Fragility Polymorphism, Genetic Phenotype Amino Acid Sequence Transcription, Genetic DNA Repair Genotype Exons Genes, Dominant DNA Replication Genome, Human Heterozygote Genetic Markers Repetitive Sequences, Amino Acid Genetic Variation Gene Frequency

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care1

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Trinucleotide Repeat Expansion Trinucleotide Repeats Friedreich Ataxia Myotonic Dystrophy DNA Repeat Expansion Spinocerebellar Degenerations Fragile X Syndrome Huntington Disease Fragile X Mental Retardation Protein Iron-Binding Proteins Alleles Mutation Repetitive Sequences, Nucleic Acid Base Sequence Spinocerebellar Ataxias Machado-Joseph Disease Molecular Sequence Data Heredodegenerative Disorders, Nervous System Nerve Tissue Proteins Genomic Instability DNA Frontotemporal Dementia Flap Endonucleases Microsatellite Repeats Anticipation, Genetic Intranuclear Inclusion Bodies Nucleic Acid Conformation Inverted Repeat Sequences Pedigree Tandem Repeat Sequences Minisatellite Repeats RNA-Binding Proteins Age of Onset Cerebellar Ataxia Polymerase Chain Reaction Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Polymorphism, Genetic Amyotrophic Lateral Sclerosis Nuclear Proteins Neurodegenerative Diseases Sequence Analysis, DNA Phenotype Proteins Amino Acid Sequence Protein-Serine-Threonine Kinases Transcription, Genetic Mice, Transgenic Peptides RNA, Messenger DNA Repair Models, Genetic DNA Primers Receptors, Androgen Genotype Myotonic Disorders Exons DNA-Binding Proteins Genes, Dominant DNA Replication Saccharomyces cerevisiae Genome, Human Myoclonic Epilepsies, Progressive Disease Models, Animal Heterozygote Genetic Markers Repetitive Sequences, Amino Acid Genetic Variation RNA MutS Homolog 2 Protein Cell Line Nucleic Acid Heteroduplexes Gene Frequency

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