𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Multimodal neurophysiological study of SCA2 and SCA3 autosomal dominant hereditary spinocerebellar ataxias

✍ Scribed by S. Álvarez-Paradelo; A. García; J. Infante; J. Berciano

Book ID
119649191
Publisher
Elsevier
Year
2011
Tongue
English
Weight
235 KB
Volume
26
Category
Article
ISSN
2173-5808

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Clinical features and neuropathology of
Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)
✍ Arndt Rolfs; Arnulf H. Koeppen; Ingrid Bauer; Peter Bauer; Sven Buhlmann; Helge 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 953 KB

Autosomal dominant spinocerebellar ataxias (SCAs) are a group of neurodegenerative disorders clinically characterized by late-onset ataxia and variable other manifestations. Genetically and clinically, SCA is highly heterogeneous. Recently, CAG repeat expansions in the gene encoding TATA-binding pro