Alleles frataxin trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy2

Intranuclear Inclusion Bodies Cell Line

Organisms2

Saccharomyces cerevisiae Mice, Transgenic

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 Drugs20

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment7

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes31

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

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

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