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Cell Line COS Cells Cells, Cultured Neurons Brain

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Mice, Transgenic Mice, Inbred C57BL Cercopithecus aethiops Escherichia coli Mice, Knockout HIV-1 Mice, Mutant Strains Saccharomyces cerevisiae Animals, Genetically Modified Drosophila melanogaster

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Disease Models, Animal Pancreatitis, Alcoholic Parkinson Disease Genetic Predisposition to Disease Gait Ataxia Gaucher Disease Genetic Diseases, Inborn Huntington Disease Neurodegenerative Diseases Syndrome

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Trypsin Inhibitor, Kazal Pancreatic Serine Glycine Glucosylceramidase Protein-Serine-Threonine Kinases DNA Primers Recombinant Proteins DNA-Binding Proteins Cysteine DNA Codon, Nonsense Carbamates Transcription Factors Codon Ethylnitrosourea Membrane Proteins RNA, Messenger Nuclear Proteins Mutant Proteins Bacterial Proteins Nerve Tissue Proteins Genetic Markers

Analytical, Diagnostic and Therapeutic Techniques and Equipment20

Animal Use Alternatives Disease Models, Animal Models, Animal Amino Acid Substitution Pedigree DNA Mutational Analysis Mutagenesis, Site-Directed Polymerase Chain Reaction Genetic Testing Models, Molecular Sequence Analysis, DNA Models, Genetic Chromosome Mapping Sequence Alignment Transfection Models, Biological Genetic Complementation Test Crystallography, X-Ray Cloning, Molecular Reverse Transcriptase Polymerase Chain Reaction

Psychiatry and Psychology1

Huntington Disease

Phenomena and Processes53

Mutation, Missense Point Mutation Mutation Amino Acid Substitution Frameshift Mutation Heterozygote Base Sequence Germ-Line Mutation Phenotype Amino Acid Sequence Alleles Homozygote Genotype Genetic Predisposition to Disease Protein Structure, Tertiary Mutagenesis Mutation Rate Exons Protein Binding Gene Frequency Binding Sites Drug Resistance, Viral Insecticide Resistance Polymorphism, Single-Stranded Conformational Sequence Homology, Amino Acid Codon, Nonsense Protein Conformation Polymorphism, Restriction Fragment Length Transfection Genes, Recessive Kinetics Genetic Linkage Sequence Deletion Haplotypes Structure-Activity Relationship Gene Deletion Genes, Dominant Suppression, Genetic Protein Structure, Secondary Virus Replication Codon Signal Transduction Founder Effect Genes, p53 Polymorphism, Single Nucleotide Genetic Variation Gene Expression Regulation Consanguinity Epistasis, Genetic Plasmids Genetic Markers Gene Expression Genes, Lethal

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Molecular Sequence Data Base Sequence Amino Acid Sequence Computer Simulation

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Genetic Testing Age of Onset

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

Animal Use Alternatives Disease Models, Animal Models, Animal Mutation, Missense Point Mutation Mutation Amino Acid Substitution Trypsin Inhibitor, Kazal Pancreatic Pedigree Frameshift Mutation Heterozygote Molecular Sequence Data DNA Mutational Analysis Pancreatitis, Alcoholic Base Sequence Germ-Line Mutation Mutagenesis, Site-Directed Phenotype Amino Acid Sequence Parkinson Disease Alleles Homozygote Genotype Jews Serine Polymerase Chain Reaction Genetic Predisposition to Disease Gait Ataxia Genetic Testing Cell Line Models, Molecular Protein Structure, Tertiary Mutagenesis Mutation Rate Gaucher Disease Sequence Analysis, DNA Glycine Exons Glucosylceramidase Protein Binding Protein-Serine-Threonine Kinases Gene Frequency DNA Primers Binding Sites Mice, Transgenic Age of Onset Drug Resistance, Viral Insecticide Resistance Polymorphism, Single-Stranded Conformational Sequence Homology, Amino Acid Romania Recombinant Proteins DNA-Binding Proteins Mice, Inbred C57BL Models, Genetic Chromosome Mapping Cysteine DNA Codon, Nonsense Carbamates Protein Conformation Sequence Alignment COS Cells Polymorphism, Restriction Fragment Length Transfection Genes, Recessive Kinetics Genetic Linkage Sequence Deletion Haplotypes Structure-Activity Relationship Gene Deletion Genes, Dominant Cercopithecus aethiops Escherichia coli Suppression, Genetic Mice, Knockout Genetic Diseases, Inborn Protein Structure, Secondary Huntington Disease Virus Replication Transcription Factors Codon Signal Transduction HIV-1 Ethylnitrosourea Cells, Cultured Membrane Proteins Models, Biological Neurodegenerative Diseases Genetic Complementation Test RNA, Messenger Nuclear Proteins Founder Effect Crystallography, X-Ray Genes, p53 Syndrome Mice, Mutant Strains Cloning, Molecular Polymorphism, Single Nucleotide

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