𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome

✍ Scribed by Belloso, Jose M; Bache, Iben; Guitart, Miriam; Caballin, Maria Rosa; Halgren, Christina; Kirchhoff, Maria; Ropers, Hans-Hilger; Tommerup, Niels; Tümer, Zeynep

Book ID
110027024
Publisher
Nature Publishing Group
Year
2007
Tongue
English
Weight
62 KB
Volume
15
Category
Article
ISSN
1018-4813

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A large Italian family with Gilles de la
A large Italian family with Gilles de la Tourette syndrome: Clinical study and analysis of the SLITRK1 gene
✍ Giovanni Fabbrini; Massimo Pasquini; Cinzia Aurilia; Isabella Berardelli; Guido 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 217 KB

## Abstract Our objective was to report the clinical characteristics and to investigate the role of __SLITRK1__ gene in a large Italian family with Tourette syndrome (TS). The diagnosis of TS and chronic motor tics (CMT) was made according to “The Tourette Syndrome Classification Study Group” (1993

No evidence for a major gene effect of t
No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian families
✍ Barr, Cathy L.; Wigg, Karen G.; Zovko, Elizabeth; Sandor, Paul; Tsui, Lap-Chee 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 31 KB 👁 3 views

Gilles de la Tourette Syndrome (TS) is a neuropsychiatric disorder characterized by both motor and vocal tics affecting approximately 1/10,000 females and 1/2000 males. Because of the success of neuroleptics and other agents interacting with the dopaminergic system in the suppression of tics, a defe