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Glucocerebrosidase gene variants in parkinsonian patients with Machado Joseph/spinocerebellar ataxia 3

✍ Scribed by M. Siebert; K.C. Donis; M. Socal; C.R.M. Rieder; V.E. Emmel; F. Vairo; K. Michelin-Tirelli; M. França Jr.; A.C. D’Abreu; C. Bettencourt; M. Lima; I. Lopes Cendes; M.L. Saraiva-Pereira; L.B. Jardim


Book ID
116821094
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
343 KB
Volume
18
Category
Article
ISSN
1353-8020

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## Abstract The cerebellar variant of multiple system atrophy (MSA‐C) has overlapping clinical features with the hereditary spinocerebellar ataxias (SCAs), but can usually be distinguished on a clinical basis. We describe a patient who developed a sporadic, late‐onset, rapidly progressive neurodege