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  • Title: Spinocerebellar ataxia with sensory neuropathy (SCA25).
    Author: Stevanin G, Broussolle E, Streichenberger N, Kopp N, Brice A, Durr A.
    Journal: Cerebellum; 2005; 4(1):58-61. PubMed ID: 15895562.
    Abstract:
    Spinocerebellar ataxia 25 (SCA25) is a rare form of autosomal dominant cerebellar ataxia associated with a severe sensory neuropathy. Clinical variability ranges from incomplete penetrance at age 61 to a Friedreich ataxia-like syndrome. The responsible locus was mapped to chromosome 2p in a large region of 14 Mbases in a single French kindred.
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