Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder.

Richard Delorme (1, 2, 3) , Catalina Betancur (2) , Michael Wagner (4) , Marie-Odile Krebs (5) , Philip Gorwood (6) , Phillip Pearl (7) , Gudrun Nygren (8) , Christelle M. Durand (1) , Friederike Buhtz (9) , P. Pickering (6) , Jonas Melke (1) , Stephan Ruhrmann (10) , Henrik Anckarsäter (8) , Nadia Chabane (2, 3) , Amélie Kipman (6) , Claudia Reck (4) , Bruno Millet (5) , Isabelle Roy (2, 11) , Marie-Christine Mouren-Simeoni (3) , Wolfgang Maier (4) , Maria Råstam (8) , Christopher Gillberg (8, 12) , Marion Leboyer (2, 11) , Thomas Bourgeron (1, 13)

1 Génétique Humaine et Fonctions Cognitives
2 Neurobiologie et Psychiatrie
3 Service de psychopathologie de l'enfant et de l'adolescent
4 Department of Psychiatry
5 Physiopathologie des Maladies Psychiatriques, Développement et Vulnérabilité
6 Analyse Phenotypique, Developpementale et Genetique des Comportements Addictifs
7 Children's National Medical Center
8 Department of Child and Adolescent Psychiatry
9 Department of Psychiatry
10 Department of Psychiatry and Psychotherapy
11 Département de Psychiatrie
12 Saint George's Hospital Medical School
13 UPD7 - Université Paris Diderot - Paris 7

No abstract available.

Domaines: Génétique

Richard Delorme, Catalina Betancur, Michael Wagner, Marie-Odile Krebs, Philip Gorwood, et al.. Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder.. Molecular Psychiatry, 2005, 10 (12), pp.1059-61. ⟨10.1038/sj.mp.4001728⟩. ⟨inserm-00125111⟩