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Article

A skeletal muscle sodium channel mutation in a Japanese family with paramyotonia congenita.

Journal of the neurological sciences - 1 Nov 1995

Yamada T, Ochi H, Hara H, Yoshimura T, Kobayashi T

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Source

Identifiers

PMID: 8583225
DOI: 10.1016/0022-510x(95)00166-y

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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A skeletal muscle sodium channel mutation in a Japanese family with paramyotonia congenita.PMID 8583225Read ↗

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Muscle sodium channel inactivation defect in paramyotonia congenita with the thr1313met mutation.Semantic proximity Read ↗

Lack of sodium channel mutation in an Italian family with paramyotonia congenita.Semantic proximity Read ↗

A novel mutation in the gene for the adult skeletal muscle sodium channel alpha-subunit (SCN4A) that causes paramyotonia congenita of von Eulenburg.Semantic proximity Read ↗

Characterization of a new sodium channel mutation at arginine 1448 associated with moderate Paramyotonia congenita in humans.Semantic proximity Read ↗

Sodium channel mutations in paramyotonia congenita exhibit similar biophysical phenotypes in vitro.Semantic proximity Read ↗

Periodic paralysis, myotonia congenita and sarcolemmal ion channels: a success of the candidate gene approach.Semantic proximity Read ↗

Sodium channel mutations and disorders of excitation in human skeletal muscle.Semantic proximity Read ↗

Genotype-phenotype correlations in human skeletal muscle sodium channel diseases.Semantic proximity Read ↗

What causes paramyotonia in the United Kingdom? Common and new SCN4A mutations revealed.Semantic proximity Read ↗

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