Homology mediate gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy2

Intranuclear Inclusion Bodies Cell Line

Organisms2

Mice, Transgenic Saccharomyces cerevisiae

Diseases19

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 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 DNA Flap Endonucleases RNA-Binding Proteins Nuclear Proteins Proteins Peptides Receptors, Androgen DNA Primers RNA, Messenger DNA-Binding Proteins Genetic Markers MutS Homolog 2 Protein Nucleic Acid Heteroduplexes Saccharomyces cerevisiae Proteins

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 Anticipation, Genetic Microsatellite Repeats Nucleic Acid Conformation Inverted Repeat Sequences Minisatellite Repeats Tandem Repeat Sequences Chromosome Fragility Amino Acid Sequence Polymorphism, Genetic Phenotype DNA Repair Sequence Homology, Amino Acid Sequence Homology, Nucleic Acid Transcription, Genetic Genotype DNA Replication Genes, Dominant Genome, Human Exons Repetitive Sequences, Amino Acid Genetic Markers Heterozygote

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 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 Anticipation, Genetic Microsatellite Repeats Nucleic Acid Conformation Inverted Repeat Sequences Minisatellite Repeats Tandem Repeat Sequences Pedigree Cerebellar Ataxia Age of Onset Intranuclear Inclusion Bodies Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Polymerase Chain Reaction RNA-Binding Proteins Genetic Diseases, Inborn Amino Acid Sequence Amyotrophic Lateral Sclerosis Polymorphism, Genetic Nuclear Proteins Neurodegenerative Diseases Proteins Peptides Sequence Analysis, DNA Phenotype DNA Repair Sequence Homology, Amino Acid Models, Genetic Receptors, Androgen Mice, Transgenic DNA Primers Sequence Homology, Nucleic Acid Transcription, Genetic Genotype Saccharomyces cerevisiae DNA Replication RNA, Messenger Genes, Dominant Genome, Human DNA-Binding Proteins Myoclonic Epilepsies, Progressive Exons Repetitive Sequences, Amino Acid Genetic Markers MutS Homolog 2 Protein Nucleic Acid Heteroduplexes Heterozygote Disease Models, Animal Cell Line Saccharomyces cerevisiae Proteins

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