## Abstract Benign hereditary chorea (BHC; OMIM 118700) is an autosomal dominant movement disorder. Mutations in the thyroid transcription factor 1 (TITF1) gene have been linked with BHC. The phenotype for BHC is highly variable and may include atypical features such as dystonia, slow saccades, and
✦ LIBER ✦
Cause and course in a series of patients with sporadic chorea
✍ Scribed by Immacolata Piccolo; Carlo Alberto Defanti; Paola Soliveri; Maria Antonietta Volontè; Giuliana Cislaghi; Floriano Girotti
- Publisher
- Springer
- Year
- 2003
- Tongue
- English
- Weight
- 192 KB
- Volume
- 250
- Category
- Article
- ISSN
- 0340-5354
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