| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8272639 | Journal of the Neurological Sciences | 2018 | 4 Pages |
Abstract
SYNE1-ataxia is, therefore, a relatively common cause of recessive ataxia characterized by complex multisystemic neurostructural changes consistent with the phenotypic heterogeneity and neuroimaging configures a potential marker of the disease.
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Authors
Maria T.D. Gama, Camila C. Piccinin, Thiago J.R. Rezende, Patrick A. Dion, Guy A. Rouleau, Marcondes C. França Junior, Orlando G.P. Barsottini, José Luiz Pedroso,