Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families.

Abstract

Autosomal dominant cerebellar ataxia type I was diagnosed in three unrelated families from Martinique (French West Indies), and linkage to the locus for spinocerebellar ataxia 2 (SCA2) was established. Neuropathological findings in two patients were those of olivopontocerebellar atrophy without oligodendroglial cytoplasmic inclusions. Cerebellar ataxia was… (More)

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@article{Drr1995AutosomalDC, title={Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families.}, author={Alexandra D{\"u}rr and David M Smadja and G{\'e}raldine Cancel and Agn{\`e}s L{\'e}zin and Giovanni Stevanin and Joanne Mikol and R{\'e}mi Bellance and Gilles Buisson and H{\'e}rve Chneiweiss and J Dellanave}, journal={Brain : a journal of neurology}, year={1995}, volume={118 ( Pt 6)}, pages={1573-81} }