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Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p

✍ Scribed by Giovanni Stevanin; Naima Bouslam; Stéphane Thobois; Hamid Azzedine; Lucas Ravaux; Anne Boland; Martin Schalling; Emmanuel Broussolle; Alexandra Dürr; Alexis Brice

Publisher: John Wiley and Sons
Year: 2003
Tongue: English
Weight: 288 KB
Volume: 55
Category: Article
ISSN: 0364-5134
DOI: 10.1002/ana.10798

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## Abstract The autosomal dominant (AD) spinocerebellar ataxias (SCAs) and hereditary sensory neuropathies (HSN) are heterogeneous disorders characterized by variable clinical, electrophysiological, and neuropathological profiles. The SCAs are clinically characterized by slowly progressive incoordi