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Article

SCA13 causes dominantly inherited non-progressive myoclonus ataxia.

Parkinsonism & related disorders - 1 May 2017

Montaut Solveig, Apartis Emmanuelle, Chanson Jean-Baptiste, Ewenczyk Claire, Renaud Mathilde, Guissart Claire, Muller Jean, Legrand André Pierre, Durr Alexandra, Laugel Vincent, Koenig Michel, Tranchant Christine, Anheim Mathieu

Abstract excerpt

INTRODUCTION: Spinocerebellar ataxia 13 (SCA13) is a rare autosomal dominant cerebellar ataxia. To our knowledge, its association to movement disorders has never been described. We aimed at reporting 8 new SCA13 cases with a focus on movement disorders especially myoclonus. METHODS: We performed a detailed neurological examination and neurophysiological recording in 8 patients consecutively diagnosed with SCA13...

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Identifiers

PMID: 28216058
DOI: 10.1016/j.parkreldis.2017.02.012

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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