Spinocerebellar ataxia with sensory neuropathy (SCA25).
Giovanni Stevanin, Emmanuel Broussolle, Nathalie Streichenberger, Nicolas Kopp, Alexis Brice, Alexandra Durr
MCER. 2005-04-01; 4(1): 58-61
DOI: 10.1080/14734220510007932
Read on PubMed
MCER. 2005-04-01; 4(1): 58-61
DOI: 10.1080/14734220510007932
Read on PubMed
1. Cerebellum. 2005;4(1):58-61.
Spinocerebellar ataxia with sensory neuropathy (SCA25).
Stevanin G(1), Broussolle E, Streichenberger N, Kopp N, Brice A, Durr A.
Author information:
(1)INSERM U679 (former U289), Federative Institute for Neuroscience Research
(IFR70), Salpetriere Hospital, Paris, France. stevanin@ccr.jussieu.fr
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.
DOI: 10.1080/14734220510007932
PMID: 15895562 [Indexed for MEDLINE]