## Abstract Mutations in the ฯตโsarcoglycan gene (SGCE) have been reported in families with myoclonusโdystonia (MโD). In addition to abnormal movements, obsessiveโcompulsive disorder (OCD) has also been described in families with MโD. OCD is a common feature in another movement disorder, namely Tour
Examination of the SLITRK1 gene in Caucasian patients with Tourette syndrome
โ Scribed by H. Deng; W. D. Le; W. J. Xie; J. Jankovic
- Book ID
- 109337493
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 92 KB
- Volume
- 114
- Category
- Article
- ISSN
- 0001-6314
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๐ SIMILAR VOLUMES
## 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 โThe Tourette Syndrome Classification Study Groupโ (1993
We report a single stranded conformational polymorphism (SSCP) analysis of the coding region of the dopamine D1 receptor (DRD1) in Tourette's syndrome (n = 50) and control (n = 50) subjects. Tourette's syndrome populations with comorbidity for attention deficit-hyperactivity disorder (AD-HD) (n = 35