A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6
✍ Scribed by Hiroki Takahashi; Kinya Ishikawa; Takeshi Tsutsumi; Hiroto Fujigasaki; Akihiro Kawata; Ryoichi Okiyama; Tsuneo Fujita; Kazuo Yoshizawa; Shigeki Yamaguchi; Hitoshi Tomiyasu; Fumihito Yoshii; Kazuko Mitani; Natsue Shimizu; Mineo Yamazaki; Tomoyuki Miyamoto; Tomoyuki Orimo; Shin’ichi Shoji; Ken Kitamura; Hidehiro Mizusawa
- Publisher
- Nature Publishing Group
- Year
- 2004
- Tongue
- English
- Weight
- 237 KB
- Volume
- 49
- Category
- Article
- ISSN
- 1435-232X
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## 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