| Literature DB >> 20445167 |
A Gulhan Ercan-Sencicek1, Althea A Stillman, Ananda K Ghosh, Kaya Bilguvar, Brian J O'Roak, Christopher E Mason, Thomas Abbott, Abha Gupta, Robert A King, David L Pauls, Jay A Tischfield, Gary A Heiman, Harvey S Singer, Donald L Gilbert, Pieter J Hoekstra, Thomas M Morgan, Erin Loring, Katsuhito Yasuno, Thomas Fernandez, Stephan Sanders, Angeliki Louvi, Judy H Cho, Shrikant Mane, Christopher M Colangelo, Thomas Biederer, Richard P Lifton, Murat Gunel, Matthew W State.
Abstract
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. 2010 Massachusetts Medical SocietyEntities:
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Year: 2010 PMID: 20445167 PMCID: PMC2894694 DOI: 10.1056/NEJMoa0907006
Source DB: PubMed Journal: N Engl J Med ISSN: 0028-4793 Impact factor: 91.245