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Article

Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13.

Epilepsia - 1 Jan 2000

Burgess D L, Matsuura T, Ashizawa T, Noebels J L

Abstract excerpt

PURPOSE: Voltage-dependent calcium channel mutations have been associated with spinocerebellar ataxia in humans (SCA6) and with ataxia, progressive cerebellar degeneration, and epilepsy in mice (tottering, lethargic, and stargazer). A novel autosomal dominant spinocerebellar ataxia syndrome with epilepsy (SCA10) was recently mapped to chromosome 22q13. The human ortholog of the mouse stargazer locus, the calcium...

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Source

Identifiers

PMID: 10643919
DOI: 10.1111/j.1528-1157.2000.tb01500.x

Genes

CACNG2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13.PMID 10643919Read ↗

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