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Article

Clinical, genetic and neuropathological characterization of spinocerebellar ataxia type 37.

Brain : a journal of neurology - 1 Jul 2018

Corral-Juan Marc, Serrano-Munuera Carmen, Rábano Alberto, Cota-González Daniel, Segarra-Roca Anna, Ispierto Lourdes, Cano-Orgaz Antonio Tomás, Adarmes Astrid D, Méndez-Del-Barrio Carlota, Jesús Silvia, Mir Pablo, Volpini Victor, Alvarez-Ramo Ramiro, Sánchez Ivelisse, Matilla-Dueñas Antoni

Abstract excerpt

The autosomal dominant spinocerebellar ataxias (SCAs) consist of a highly heterogeneous group of rare movement disorders characterized by progressive cerebellar ataxia variably associated with ophthalmoplegia, pyramidal and extrapyramidal signs, dementia, pigmentary retinopathy, seizures, lower motor neuron signs, or peripheral neuropathy. Over 41 different SCA subtypes have been described evidencing the high...

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Identifiers

PMID: 29939198
DOI: 10.1093/brain/awy137

Genes

DAB1

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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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