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Article

A novel mutation of the CLCN1 gene associated with myotonia hereditaria in an Australian cattle dog.

Journal of veterinary internal medicine - 1 Jan 2000

Finnigan Daniel F, Hanna W J Brad, Poma Roberto, Bendall Andrew J

Abstract excerpt

BACKGROUND: Heritable myotonia is a genetic muscle disorder characterized by slow relaxation of skeletal muscles. The main clinical signs are skeletal muscle stiffness, especially after vigorous contraction, and muscle hypertrophy. Muscle stiffness may be enhanced by inactivity, and often is relieved by exercise. Myotonia can be inherited in an autosomal dominant or recessive manner (Thomsen- or Becker-type...

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Source

Identifiers

PMID: 17552451
DOI: 10.1892/0891-6640(2007)21[458:anmotc]2.0.co;2

Genes

CLCN1

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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