## Abstract Benign hereditary chorea (BHC) is a rare autosomal dominant nonprogressive movement disorder. In some cases the phenotype includes, besides choreoathetosis, thyroid dysfunction and pulmonary infections in infancy, as expressed by the name “Brain‐Thyroid‐Lung syndrome”. Mutations in the
✦ LIBER ✦
Nonsense mutation inTITF1in a Portuguese family with benign hereditary chorea
✍ Scribed by Maria do Carmo Costa; Cristina Costa; Ana Paula Silva; Pedro Evangelista; Luís Santos; Anabela Ferro; Jorge Sequeiros; Patrícia Maciel
- Publisher
- Springer
- Year
- 2005
- Tongue
- English
- Weight
- 376 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1364-6745
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