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Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3

✍ Scribed by K. Bürk; M. Fetter; M. Abele; F. Laccone; A. Brice; J. Dichgans; T. Klockgether


Publisher
Springer
Year
1999
Tongue
English
Weight
140 KB
Volume
246
Category
Article
ISSN
0340-5354

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The autosomal dominant cerebellar ataxias (ADCA) are clinically and genetically heterogeneous. To date, several loci (SCAI-V) have been identified for ADCA type I. We have studied two large families from the northern part of The Netherlands with ADCA type I with a broad intra-familial variation of s