Gender characterization in a large series of Brazilian patients with spondyloarthritis
✍ Scribed by Hellen M. S. de Carvalho; Adriana B. Bortoluzzo; Célio R. Gonçalves; José Antonio Braga da Silva; Antonio Carlos Ximenes; Manoel B. Bértolo; Sandra L. E. Ribeiro; Mauro Keiserman; Rita Menin; Thelma L. Skare; Sueli Carneiro; Valderílio F. Azevedo; Walber P. Vieira; Elisa N. Albuquerque; Washington A. Bianchi; Rubens Bonfiglioli; Cristiano Campanholo; Izaias P. Costa; Angela P. Duarte; Maria Bernadete O. Gavi; Charles L. Kohem; Nocy H. Leite; Sonia A. L. Lima; Eduardo S. Meirelles; Ivânio A. Pereira; Marcelo M. Pinheiro; Elizandra Polito; Gustavo G. Resende; Francisco Airton C. Rocha; Mittermayer B. Santiago; Maria de Fátima L. C. Sauma; Percival D. Sampaio-Barros; from the Brazilian Registry on Spondyloarthritis
- Book ID
- 113056194
- Publisher
- Springer
- Year
- 2011
- Tongue
- English
- Weight
- 176 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0770-3198
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## Abstract Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder caused by an ATTCT repeat intronic expansion in the SCA10 gene. SCA 10 has been reported in Mexican, Brazilian, Argentinean and Venezuelan families. Its phenotype is overall characterized by cerebellar ataxia and e