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Article

A novel sodium channel mutation in a family with hypokalemic periodic paralysis.

Neurology - 10 Dec 1999

Bulman D E, Scoggan K A, van Oene M D, Nicolle M W, Hahn A F, Tollar L L, Ebers G C

Abstract excerpt

OBJECTIVE: To identify the cause of hypokalemic periodic paralysis (HOKPP) in a family whose disease is not caused by a mutation in the dihydropyridine-sensitive (DHP) receptor alpha1-subunit gene (CACNA1S). BACKGROUND: Hypokalemic periodic paralysis is primarily caused by mutations within CACNA1S. Genetic heterogeneity for HOKPP has been reported, but no other locus has been identified. METHODS: Single-stranded...

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Source

Identifiers

PMID: 10599760
DOI: 10.1212/wnl.53.9.1932

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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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