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

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Anatomy3

Intranuclear Inclusion Bodies Cell Line Chromosomes, Human, X

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 Diseases, Inborn Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Amyotrophic Lateral Sclerosis Neurodegenerative Diseases Disease Models, Animal Myoclonic Epilepsies, Progressive Ataxia

Chemicals and Drugs20

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

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

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes40

Trinucleotide Repeat Expansion Trinucleotide Repeats DNA Repeat Expansion Alleles Mutation Base Sequence Repetitive Sequences, Nucleic Acid Point Mutation Mutation, Missense Genomic Instability Microsatellite Repeats Anticipation, Genetic Nucleic Acid Conformation Tandem Repeat Sequences Inverted Repeat Sequences Minisatellite Repeats Chromosome Fragility Polymorphism, Genetic Amino Acid Sequence Phenotype Exons Genotype Heterozygote Transcription, Genetic DNA Repair Genes, Dominant Frameshift Mutation Genetic Variation DNA Replication Genetic Markers Gene Frequency Sequence Deletion Genome, Human Promoter Regions, Genetic Germ-Line Mutation Recombination, Genetic Repetitive Sequences, Amino Acid Genetic Linkage Gene Expression Chromosomes, Human, X

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care2

Age of Onset Genetic Testing

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 Base Sequence Repetitive Sequences, Nucleic Acid Molecular Sequence Data Spinocerebellar Ataxias Point Mutation Machado-Joseph Disease Pedigree Heredodegenerative Disorders, Nervous System Nerve Tissue Proteins DNA Mutation, Missense Genomic Instability Microsatellite Repeats Polymerase Chain Reaction Frontotemporal Dementia Flap Endonucleases Anticipation, Genetic Nucleic Acid Conformation Tandem Repeat Sequences Age of Onset Inverted Repeat Sequences Minisatellite Repeats Cerebellar Ataxia Intranuclear Inclusion Bodies Sequence Analysis, DNA Genetic Diseases, Inborn Chromosome Fragility RNA-Binding Proteins Polymorphism, Genetic Muscular Dystrophy, Oculopharyngeal Amino Acid Sequence Phenotype Nuclear Proteins Exons Genotype Heterozygote Amyotrophic Lateral Sclerosis Proteins DNA Primers Transcription, Genetic Neurodegenerative Diseases Models, Genetic DNA Repair Genes, Dominant Peptides Mice, Transgenic DNA Mutational Analysis Frameshift Mutation RNA, Messenger DNA-Binding Proteins Saccharomyces cerevisiae Receptors, Androgen Chromosome Mapping Genetic Variation Cell Line DNA Replication Genetic Markers Gene Frequency Sequence Deletion Genome, Human Promoter Regions, Genetic Genetic Testing MutS Homolog 2 Protein Germ-Line Mutation Transcription Factors Saccharomyces cerevisiae Proteins Disease Models, Animal Myoclonic Epilepsies, Progressive Recombination, Genetic Repetitive Sequences, Amino Acid Cloning, Molecular Nucleic Acid Heteroduplexes Genetic Linkage RNA Ataxia Gene Expression Chromosomes, Human, X Oligodeoxyribonucleotides

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