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Article

Recent developments in the molecular genetics of malignant hyperthermia: implications for future diagnosis at the DNA level.

Acta anaesthesiologica Belgica - 1 Jan 1990

McCarthy T V, Healy J M, Lehane M, Heffron J J

Abstract excerpt

Molecular genetic linkage studies on the inherited human disorder malignant hyperthermia have resulted in the mapping of the locus for malignant hyperthermia susceptibility (MHS) to the twenty centimorgan genetic interval in the q12-13.2 region of chromosome 19 defined by the anonymous polymorphic DNA markers D19S9 and BCL3. The mapping of the MHS locus to this interval now allows diagnosis of MHS in selected...

Topics

Chromosomes, Human, Pair 19
Genetic Markers
Genotype
Humans
Malignant Hyperthermia
Polymorphism, Restriction Fragment Length

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 1973552

Genes

BCL3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-1973552-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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