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Epilepsy as the symptom of a spinocerebellar ataxia 13 in a patient presenting with a mutation in the KCNC3 gene

BACKGROUND: The spinocerebellar ataxias (SCAs) refer to a diverse group of neurodegenerative illnesses that vary clinically and genetically. One of the rare subtypes within this group is SCA13, caused by mutations in the KCNC3 gene. Currently, the prevalence of SCA13 remains uncertain, with only a c...

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Detalles Bibliográficos
Autores principales: Li, Shao, Shang, Dandan, Du, Yanjiao, Li, Yan, Liu, Ruihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294460/
https://www.ncbi.nlm.nih.gov/pubmed/37365508
http://dx.doi.org/10.1186/s12883-023-03304-5

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