Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy (Amadori E et al., 2022)

Eur J Med Genet. 2022 Dec;65(12):104633. doi: 10.1016/j.ejmg.2022.104633. Epub 2022 Oct 4.

Authors

José Gazulla¹, Silvia Izquierdo-Alvarez², José Berciano³

Affiliations

¹ Department of Neurology, Hospital Universitario Miguel Servet, Spain. Electronic address: josegazulla@gmail.com.
² Section of Genetics, Department of Clinical Biochemistry, Hospital Universitario Miguel Servet, Isabel la Católica, 1-3, 50009, Zaragoza, Spain.
³ Department of Neurology, Hospital Universitario Marqués de Valdecilla (IDIVAL), University of Cantabria, CIBERNED, Santander, Spain.

PMID: 36206970
DOI: 10.1016/j.ejmg.2022.104633

No abstract available

Keywords: Autosomal dominant; CACNA1G; Epilepsy; Episodic ataxia; Episodic vestibulocerebellar ataxia; T-type voltage-gated calcium channel.

Publication types

Letter
Comment

MeSH terms

Ataxia* / genetics
Epilepsy* / genetics
Humans

Supplementary concepts

Episodic Ataxia