Polymorphic gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy1

Intranuclear Inclusion Bodies

Organisms2

Mice, Transgenic Saccharomyces cerevisiae

Diseases20

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

Chemicals and Drugs17

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment6

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes36

Trinucleotide Repeat Expansion Trinucleotide Repeats DNA Repeat Expansion Alleles Polymorphism, Genetic Mutation Repetitive Sequences, Nucleic Acid Base Sequence Genotype Genomic Instability Anticipation, Genetic Microsatellite Repeats Nucleic Acid Conformation Genetic Variation Inverted Repeat Sequences Minisatellite Repeats Tandem Repeat Sequences Haplotypes Genetic Predisposition to Disease Gene Frequency Chromosome Fragility Genetic Markers Genetic Linkage Amino Acid Sequence Major Histocompatibility Complex Phenotype DNA Repair Polymorphism, Single Nucleotide Selection, Genetic Genes, Dominant DNA Replication Genome, Human Transcription, Genetic Repetitive Sequences, Amino Acid Heterozygote Exons

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care1

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

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

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