Huntington. Medical search. Frequent questions

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Anatomy9

Chromosomes, Human, Pair 4 Corpus Striatum Caudate Nucleus Brain Neostriatum Nerve Fibers, Unmyelinated Neurons Inclusion Bodies Putamen

Organisms2

Rats, Transgenic Mice, Transgenic

Diseases9

Huntington Disease Chorea Prodromal Symptoms Disease Models, Animal Neurodegenerative Diseases Atrophy Neuroacanthocytosis Disease Progression Nerve Degeneration

Chemicals and Drugs11

Nerve Tissue Proteins Nuclear Proteins Quinolinic Acid 3-Hydroxyanthranilate 3,4-Dioxygenase Tetrabenazine Quinolinic Acids Peptides Dopamine and cAMP-Regulated Phosphoprotein 32 Mutant Proteins Genetic Markers Nitro Compounds

Analytical, Diagnostic and Therapeutic Techniques and Equipment12

Prodromal Symptoms Disease Models, Animal Witchcraft Genetic Testing Rotarod Performance Test Pedigree Chromosome Banding Gene Knock-In Techniques Heterozygote Detection Early Diagnosis Magnetic Resonance Imaging Chromosome Mapping

Psychiatry and Psychology1

Huntington Disease

Phenomena and Processes11

Trinucleotide Repeat Expansion Trinucleotide Repeats Chromosomes, Human, Pair 4 Mutation Lipoylation Phenotype Genetic Markers Alleles Genetic Linkage Genotype Autophagy

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Humanities1

Health Care3

Age of Onset Genetic Testing Genetic Counseling

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Humanities Health Care

Huntington Disease Trinucleotide Repeat Expansion Trinucleotide Repeats Chromosomes, Human, Pair 4 Nerve Tissue Proteins Nuclear Proteins Quinolinic Acid Corpus Striatum Age of Onset 3-Hydroxyanthranilate 3,4-Dioxygenase Chorea Prodromal Symptoms Rats, Transgenic Disease Models, Animal Neurodegenerative Diseases Witchcraft Genetic Testing Caudate Nucleus Atrophy Tetrabenazine Mice, Transgenic Brain Rotarod Performance Test Mutation Neostriatum Mythology Quinolinic Acids Neuroacanthocytosis Peptides Nerve Fibers, Unmyelinated Neurons Inclusion Bodies Putamen Pedigree Lipoylation Chromosome Banding Gene Knock-In Techniques Genetic Counseling Phenotype Dopamine and cAMP-Regulated Phosphoprotein 32 Mutant Proteins Genetic Markers Alleles Disease Progression Genetic Linkage Nitro Compounds Heterozygote Detection Early Diagnosis Magnetic Resonance Imaging Genotype Nerve Degeneration Chromosome Mapping Autophagy

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