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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Spinocerebellar ataxia with sensory neuropathy (SCA25).

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.[1]

References

  1. Spinocerebellar ataxia with sensory neuropathy (SCA25). Stevanin, G., Broussolle, E., Streichenberger, N., Kopp, N., Brice, A., Durr, A. Cerebellum (2005) [Pubmed]
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