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Article

Ataxia plus myoclonus in a 23-year-old patient due to STUB1 mutations.

Neurology - 15 Jul 2014

Cordoba Marta, Rodriguez-Quiroga Sergio, Gatto Emilia Mabel, Alurralde Agustín, Kauffman Marcelo Andrés

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Share to Ataxia
Share to Genetic Neurodegenerative Diseases
Share to Glycogen Storage Diseases and Myoclonus
Share to Microtubule and mitosis dynamics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 24928119
DOI: 10.1212/WNL.0000000000000600

Genes

STUB1

Provenance

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Related research

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Ataxia plus myoclonus in a 23-year-old patient due to STUB1 mutations.PMID 24928119Read ↗

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