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“Pseudodominant inheritance” of ataxia with ocular apraxia type 2 (AOA2)

✍ Scribed by L. Schöls; L. Arning; R. Schüle; J. T. Epplen; D. Timmann

Publisher
Springer
Year
2008
Tongue
English
Weight
370 KB
Volume
255
Category
Article
ISSN
0340-5354

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## Abstract Spinocerebellar ataxia type 2 (SCA2) has been recognized recently as an uncommon cause of parkinsonism, an alternate presentation to the typical cerebellar disorder. This research review summarizes the existing literature on parkinsonism‐predominant presentation SCA2 and presents new cl