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Nigrostriatal involvement in ataxia with oculomotor apraxia type 1

✍ Scribed by E. Salvatore; A. Varrone; C. Criscuolo; P. Mancini; V. Sansone; C. Strisciuglio; D. Cicala; V. Scarano; M. Salvatore; S. Pappatà; G. De Michele; A. Filla


Publisher
Springer
Year
2007
Tongue
English
Weight
258 KB
Volume
255
Category
Article
ISSN
0340-5354

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Autosomal recessive ataxias are heterogeneous group of disorders characterized by cerebellar atrophy and peripheral sensorimotor neuropathy. Molecular characterization of this group of disorders identified a number of genes contributing to these overlapping phenotypes. Ataxia with oculomotor apraxia