
pmid: 20445167
pmc: PMC2894694
Tourette's syndrome is a common developmental neuropsychiatric disorder characterized by chronic motor and vocal tics. Despite a strong genetic contribution, inheritance is complex, and risk alleles have proven difficult to identify. Here, we describe an analysis of linkage in a two-generation pedigree leading to the identification of a rare functional mutation in the HDC gene encoding L-histidine decarboxylase, the rate-limiting enzyme in histamine biosynthesis. Our findings, together with previously published data from model systems, point to a role for histaminergic neurotransmission in the mechanism and modulation of Tourette's syndrome and tics.
Male, Genetic Linkage, Chromosome Mapping, Histidine Decarboxylase, EFFICACY, Polymerase Chain Reaction, Pedigree, GENOME, MICE, Haplotypes, Codon, Nonsense, HISTAMINE, SCHIZOPHRENIA, COGNITION, Humans, Female, Genetic Predisposition to Disease, Genes, Dominant, Microsatellite Repeats, Tourette Syndrome
Male, Genetic Linkage, Chromosome Mapping, Histidine Decarboxylase, EFFICACY, Polymerase Chain Reaction, Pedigree, GENOME, MICE, Haplotypes, Codon, Nonsense, HISTAMINE, SCHIZOPHRENIA, COGNITION, Humans, Female, Genetic Predisposition to Disease, Genes, Dominant, Microsatellite Repeats, Tourette Syndrome
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