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Article

A homozygous KCNJ10 mutation in Jack Russell Terriers and related breeds with spinocerebellar ataxia with myokymia, seizures, or both.

Journal of veterinary internal medicine - 1 Jan 2000

Gilliam D, O'Brien D P, Coates J R, Johnson G S, Johnson G C, Mhlanga-Mutangadura T, Hansen L, Taylor J F, Schnabel R D

Abstract excerpt

BACKGROUND: Juvenile-onset spinocerebellar ataxia has been recognized in Jack Russell Terriers and related Russell group terriers (RGTs) for over 40 years. Ataxia occurs with varying combinations of myokymia, seizures, and other signs of neurologic disease. More than 1 form of the disease has been suspected. HYPOTHESIS/OBJECTIVES: The objective was to identify the mutation causing the spinocerebellar ataxia...

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Source

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Identifiers

PMID: 24708069
DOI: 10.1111/jvim.12355
PMCID: PMC4238845

Genes

KCNJ10

Variants

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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